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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Vydáno v:Mol Vis
Hlavní autoři: Rauf, Bushra, Irum, Bushra, Khan, Shahid Y., Kabir, Firoz, Naeem, Muhammad Asif, Riazuddin, Sheikh, Ayyagari, Radha, Riazuddin, S. Amer
Médium: Artigo
Jazyk:Inglês
Vydáno: Molecular Vision 2020
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7043638/
https://ncbi.nlm.nih.gov/pubmed/32165823
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