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...

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Bibliografske podrobnosti
izdano v:Mol Vis
Main Authors: Rauf, Bushra, Irum, Bushra, Khan, Shahid Y., Kabir, Firoz, Naeem, Muhammad Asif, Riazuddin, Sheikh, Ayyagari, Radha, Riazuddin, S. Amer
Format: Artigo
Jezik:Inglês
Izdano: Molecular Vision 2020
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7043638/
https://ncbi.nlm.nih.gov/pubmed/32165823
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