Nalaganje...

Novel mutation of GJA8 in autosomal dominant congenital cataracts

BACKGROUND: Congenital cataracts is the most common cause of childhood visual impairment and blindness worldwide. It is reported that about one quarter of congenital cataracts caused by genetic defects. Various gene mutations have been identified in hereditary cataracts so far. The purpose of the pr...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Ann Transl Med
Main Authors: Ding, Ning, Chen, Zhengyu, Song, Xudong, Tang, Xiaoyan
Format: Artigo
Jezik:Inglês
Izdano: AME Publishing Company 2020
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7576067/
https://ncbi.nlm.nih.gov/pubmed/33240976
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm-20-4663
Oznake: Označite
Brez oznak, prvi označite!