A carregar...

A 556 kb deletion in the downstream region of the PAX6 gene causes familial aniridia and other eye anomalies in a Chinese family

PURPOSE: The paired box gene 6 (PAX6) on human chromosome 11p13 is an essential transcription factor for eye formation in animals. Mutations in PAX6 can lead to varieties of autosomal-dominant ocular malformations with aniridia as the major clinical signs. Known genetic alterations causing haplo-ins...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Cheng, Fang, Song, Wulian, Kang, Yang, Yu, Shihui, Yuan, Huiping
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3038207/
https://ncbi.nlm.nih.gov/pubmed/21321669
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!