Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma

BACKGROUND: Primary congenital glaucoma (PCG) is the most common form of glaucoma in children. PCG occurs due to the developmental defects in the trabecular meshwork and anterior chamber of the eye. The purpose of this study is to identify the causative genetic variants in three families with develo...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:PLoS One
Päätekijät: Micheal, Shazia, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Iqbal, Aftab, Khan, Muhammad Imran, den Hollander, Anneke I.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2016
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4943665/
https://ncbi.nlm.nih.gov/pubmed/27409795
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0159259
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