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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Mol Vis
Prif Awduron: Rauf, Bushra, Irum, Bushra, Khan, Shahid Y., Kabir, Firoz, Naeem, Muhammad Asif, Riazuddin, Sheikh, Ayyagari, Radha, Riazuddin, S. Amer
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Molecular Vision 2020
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7043638/
https://ncbi.nlm.nih.gov/pubmed/32165823
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