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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Détails bibliographiques
Publié dans:Mol Vis
Auteurs principaux: Rauf, Bushra, Irum, Bushra, Khan, Shahid Y., Kabir, Firoz, Naeem, Muhammad Asif, Riazuddin, Sheikh, Ayyagari, Radha, Riazuddin, S. Amer
Format: Artigo
Langue:Inglês
Publié: Molecular Vision 2020
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC7043638/
https://ncbi.nlm.nih.gov/pubmed/32165823
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