Novel mutations in LTBP2 identified in familial cases of primary congenital glaucoma

PURPOSE: Primary congenital glaucoma (PCG) is a genetically heterogeneous disorder caused by developmental defects in the anterior chamber and trabecular meshwork. This disease is an important cause of childhood blindness. In this study, we aim to identify the genetic determinants of PCG in three co...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Mol Vis
Main Authors: Rauf, Bushra, Irum, Bushra, Khan, Shahid Y., Kabir, Firoz, Naeem, Muhammad Asif, Riazuddin, Sheikh, Ayyagari, Radha, Riazuddin, S. Amer
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2020
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7043638/
https://ncbi.nlm.nih.gov/pubmed/32165823
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados