Condition: Vitelliform Macular Dystrophy


rs121918288 in BEST1 gene and Vitelliform Macular Dystrophy PMID 21330666 2011 Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathy.

PMID 10331951 1999 Bestrophin gene mutations in patients with Best vitelliform macular dystrophy.

PMID 12324875 2002 Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophy.

PMID 18400985 2008 Bestrophin Cl- channels are highly permeable to HCO3-.

PMID 15176385 2004 Gene Symbol: VMD2. Disease: Best vitelliform macular dystrophy (VMD2).

PMID 19357557 2009 Clinical and molecular genetic analysis of best vitelliform macular dystrophy.

PMID 12187431 2002 Identification of a novel VMD2 mutation in Japanese patients with Best disease.

PMID 13129869 2003 Phenotype and genotype correlations in two best families.

PMID 18766995 2008 Mutation analysis of the VMD2 gene in thai families with best macular dystrophy.

PMID 10682987 2000 A novel spontaneous missense mutation in VMD2 gene is a cause of a best macular dystrophy sporadic case.

PMID 10453731 1999 Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies.

PMID 10394929 1999 The mutation spectrum of the bestrophin protein--functional implications.

PMID 14517959 2003 Ten novel mutations in VMD2 associated with Best macular dystrophy (BMD).

PMID 11449320 2001 Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene.

PMID 11241846 2001 Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy.

PMID 10798642 2000 Allelic variation in the VMD2 gene in best disease and age-related macular degeneration.

PMID 9662395 1998 Identification of the gene responsible for Best macular dystrophy.

PMID 9700209 1998 Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease).

PMID 22234150 2012 Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies).

PMID 11241846 2001 ABSTRACT We report five novel VMD2 mutations in Best's macular dystrophy patients (S16F, I73N, R92H, V235L, and N296S).

PMID 11756879 2001 Visual outcome following subretinal hemorrhage in Best disease.

PMID 30718709 2019 Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.

rs121918284 in BEST1;LOC107984334 gene and Vitelliform Macular Dystrophy PMID 21330666 2011 Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathy.

PMID 11449320 2001 Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene.

PMID 15176385 2004 Gene Symbol: VMD2. Disease: Best vitelliform macular dystrophy (VMD2).

PMID 18766995 2008 Mutation analysis of the VMD2 gene in thai families with best macular dystrophy.

PMID 11241846 2001 Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy.

PMID 13129869 2003 Phenotype and genotype correlations in two best families.

PMID 19357557 2009 Clinical and molecular genetic analysis of best vitelliform macular dystrophy.

PMID 10798642 2000 Allelic variation in the VMD2 gene in best disease and age-related macular degeneration.

PMID 14517959 2003 Ten novel mutations in VMD2 associated with Best macular dystrophy (BMD).

PMID 18400985 2008 Bestrophin Cl- channels are highly permeable to HCO3-.

PMID 9662395 1998 Identification of the gene responsible for Best macular dystrophy.

PMID 10331951 1999 Bestrophin gene mutations in patients with Best vitelliform macular dystrophy.

PMID 12187431 2002 Identification of a novel VMD2 mutation in Japanese patients with Best disease.

PMID 9700209 1998 Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease).

PMID 12324875 2002 Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophy.

PMID 10394929 1999 The mutation spectrum of the bestrophin protein--functional implications.

PMID 10453731 1999 Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies.

PMID 10682987 2000 A novel spontaneous missense mutation in VMD2 gene is a cause of a best macular dystrophy sporadic case.

PMID 22234150 2012 Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies).

PMID 30718709 2019 Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.

PMID 11241846 2001 ABSTRACT We report five novel VMD2 mutations in Best's macular dystrophy patients (S16F, I73N, R92H, V235L, and N296S).

rs752125512 in FTH1;BEST1 gene and Vitelliform Macular Dystrophy PMID 24560797 2014 Disease-causing mutations associated with four bestrophinopathies exhibit disparate effects on the localization, but not the oligomerization, of Bestrophin-1.

PMID 21467170 2011 A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive mode.

rs1565036465 in LOC107984334;BEST1 gene and Vitelliform Macular Dystrophy PMID 18703557 2008 A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene.

PMID 19357557 2009 Clinical and molecular genetic analysis of best vitelliform macular dystrophy.

PMID 10682987 2000 A novel spontaneous missense mutation in VMD2 gene is a cause of a best macular dystrophy sporadic case.

PMID 18766995 2008 Mutation analysis of the VMD2 gene in thai families with best macular dystrophy.

PMID 10331951 1999 Bestrophin gene mutations in patients with Best vitelliform macular dystrophy.

PMID 10394929 1999 The mutation spectrum of the bestrophin protein--functional implications.

PMID 10798642 2000 Allelic variation in the VMD2 gene in best disease and age-related macular degeneration.

PMID 11241846 2001 Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy.

PMID 12187431 2002 Identification of a novel VMD2 mutation in Japanese patients with Best disease.

PMID 10453731 1999 Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies.

PMID 11449320 2001 Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene.

PMID 18400985 2008 Bestrophin Cl- channels are highly permeable to HCO3-.

PMID 14517959 2003 Ten novel mutations in VMD2 associated with Best macular dystrophy (BMD).

PMID 9662395 1998 Identification of the gene responsible for Best macular dystrophy.

PMID 13129869 2003 Phenotype and genotype correlations in two best families.

PMID 15176385 2004 Gene Symbol: VMD2. Disease: Best vitelliform macular dystrophy (VMD2).

PMID 9700209 1998 Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease).

PMID 21330666 2011 Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathy.

PMID 12324875 2002 Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophy.

PMID 11241846 2001 ABSTRACT We report five novel VMD2 mutations in Best's macular dystrophy patients (S16F, I73N, R92H, V235L, and N296S).

PMID 11241846 2001 ABSTRACT We report five novel VMD2 mutations in Best's macular dystrophy patients (S16F, I73N, R92H, V235L, and N296S).

PMID 30718709 2019 Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.

PMID 19357557 2009 However, the p.Ala243Val seems to cause a mild and relatively invariable BVMD phenotype.

PMID 22234150 2012 Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies).

rs61755797 in PRPH2 gene and Vitelliform Macular Dystrophy PMID 30718709 2019 Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.