Condition: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3
rs28942068 in
POMGNT1;TSPAN1 gene and
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3
PMID 19067344 2008 Brain involvement in muscular dystrophies with defective dystroglycan glycosylation.
PMID 12788071 2003 Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease.
PMID 15207699 2004 Structure-function analysis of human protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase 1, POMGnT1.
PMID 15236414 2004 POMGnT1 gene alterations in a family with neurological abnormalities.
PMID 15466003 2004 POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease.
PMID 17030669 2006 POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum.
PMID 11709191 2001 Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
PMID 12588800 2003 Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease.
PMID 21078917 2010 Consensus statement on standard of care for congenital muscular dystrophies.
rs193919335 in
TSPAN1;POMGNT1 gene and
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3
PMID 15207699 2004 Structure-function analysis of human protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase 1, POMGnT1.
PMID 12588800 2003 Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease.
PMID 15466003 2004 POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease.
PMID 15236414 2004 POMGnT1 gene alterations in a family with neurological abnormalities.
PMID 11709191 2001 Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
PMID 17030669 2006 POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum.
PMID 12788071 2003 Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease.
PMID 19067344 2008 Brain involvement in muscular dystrophies with defective dystroglycan glycosylation.
PMID 21078917 2010 Consensus statement on standard of care for congenital muscular dystrophies.