Lack of association of the WRN C1367T polymorphism with senile cataract in the Israeli population

PURPOSE: Werner syndrome is an autosomal recessive disease of premature aging caused by a polymorphic C1367T mutation in the Werner (WRN) gene. Although there are differences between the pathobiology of normal aging and the phenotype of Werner syndrome, the clinical age-related changes are similar....

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Detalles Bibliográficos
Autores principales: Ehrenberg, M., Dratviman-Storobinsky, O., Avraham-Lubin, B.R., Goldenberg-Cohen, N.
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2929941/
https://www.ncbi.nlm.nih.gov/pubmed/20808731

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2929941/
https://www.ncbi.nlm.nih.gov/pubmed/20808731

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