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....

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Ehrenberg, M., Dratviman-Storobinsky, O., Avraham-Lubin, B.R., Goldenberg-Cohen, N.
Формат: Artigo
Язык:Inglês
Опубликовано: Molecular Vision 2010
Предметы:
Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2929941/
https://ncbi.nlm.nih.gov/pubmed/20808731
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы