Genetic analysis of Usher syndrome associated genes in Iranian pedigrees: The prominent role of MYO7A gene
Author:
Funder
Shiraz University of Medical Sciences
Publisher
Elsevier BV
Subject
Genetics
Reference23 articles.
1. Diversity of the genes implicated in Algerian patients affected by Usher syndrome;Abdi;PLoS One,2016
2. CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness;Astuto;Am. J. Hum. Genet.,2002
3. A deletion mutation in SANS results in atypical Usher syndrome;Bashir;Clin. Genet.,2010
4. Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle;Boëda;EMBO J.,2002
5. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D;Bolz;Nat. Genet.,2001
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