Condition: Werner Syndrome


rs113993961 in WRN gene and Werner Syndrome PMID 9225981 1997 Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population.

PMID 8602509 1996 Positional cloning of the Werner's syndrome gene.

PMID 10347997 1999 Prevalence of Werner's syndrome heterozygotes in Japan.

PMID 10543396 1999 Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products.

PMID 16673358 2006 The spectrum of WRN mutations in Werner syndrome patients.

PMID 9012406 1997 Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

PMID 15888165 2005 A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay.

PMID 25182132 2015 Clinical utility gene card for: Werner Syndrome--Update 2014.

PMID 8968742 1996 Homozygous and compound heterozygous mutations at the Werner syndrome locus.

PMID 25390333 2014 Reprogramming suppresses premature senescence phenotypes of Werner syndrome cells and maintains chromosomal stability over long-term culture.

PMID 16786514 2006 Werner syndrome and mutations of the WRN and LMNA genes in France.

PMID 22188495 2012 A WS patient with an Arg987Ter mutation has been previously reported in Switzerland, the present case is the first to be identified in Asia.

PMID 20443122 2010 WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.

PMID 18810497 2008 The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.