The function of the dna helicase encoded by wrn, the gene responsible for ws.
47+ Werner Syndrome Wrn Gene Pics. Werner's syndrome (ws) is an extremely rare, autosomal recessive, systemic disease which is associated with features of premature aging and cancer predisposition. Werner syndrome is named after the german scientist otto werner.
Werner Syndrome | Semantic Scholar from d3i71xaburhd42.cloudfront.net
Werner syndrome is known to be autosomal and recessive, which can be passed from one generation to another within a family, by copying one of the genes from each parent. Werner syndrome is caused by mutations in the wrn gene and is inherited in an autosomal recessive manner. Lmna (lamin a/c) gene mutation has been wrn mutations in werner syndrome patients:
A rare, autosomal recessive syndrome caused by mutations in the wrn gene.
Werner syndrome is a genetic condition. Research of werner syndrome has been linked to premature aging syndrome, malignant neoplasms, progeria, neoplasms, genomic these pathways complement our catalog of research reagents for the study of werner syndrome including antibodies and elisa kits against wrn, blm. Otto werner originally defined werner syndrome (ws) in 1904 on the basis of sclerodermalike, thin 14 most are associated with defects in genome maintenance. Werner syndrome is transmitted as an autosomal recessive trait.
