Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1

PURPOSE: This study investigated the genetic basis for Usher syndrome type 1 (USH1) in four consanguineous Israeli Arab families. METHODS: Haplotype analysis for all known USH1 loci was performed in each family. In families for which haplotype analysis was inconclusive, we performed genome-wide homo...

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Hlavní autoři: Rizel, Leah, Safieh, Christine, Shalev, Stavit A., Mezer, Eedy, Jabaly-Habib, Haneen, Ben-Neriah, Ziva, Chervinsky, Elena, Briscoe, Daniel, Ben-Yosef, Tamar
Médium: Artigo
Jazyk:Inglês
Vydáno: Molecular Vision 2011
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3250379/
https://ncbi.nlm.nih.gov/pubmed/22219650
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