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Fatemeh Arab | OMICS International
ISSN: 2472-128X

Journal of Clinical & Medical Genomics
Open Access

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Fatemeh Arab

Iran
Publications

Three Novel CYP1B1 Mutations (p.L480P, p.S476P, p.R175P) in Primary Congenital Glaucoma Cases Residing in Eastern Iran

Background purpose: Primary Congenital Glaucoma (PCG) is typically an autosomal recessive trait and is more prevalent in community with consanguineous marriage. The aim of current study was to screen 27 familial cases of PCG for CYP1B1, to identify and determine common mutations, and to understand its penetrance and prevalence in the Eastern provin... Read More»

Fatemeh Arab, Esmat Rigi Yousefabadi, Ramin Daneshvar and Ehsan Ghayoor Karimiani

: J Clin Med Genomics 2016, 7: 157

Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article

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