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A Novel De Novo Dominant Mutation in GJB2 Gene Associated with a Sporadic Case of Nonsyndromic Sensorineural Hearing Loss

Mutations in the GJB2 gene are the most common known cause of hereditary congenital hearing loss. Rapid genomic DNA extraction (RGDE) method was used for genomic DNA extraction. After amplification of coding region of CX26 gene with specific primers, expected PCR products with 724bp length were subj...

詳細記述

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書誌詳細
出版年:Iran J Public Health
主要な著者: ONSORI, Habib, RAHMATI, Mohammad, FAZLI, Davood
フォーマット: Artigo
言語:Inglês
出版事項: Tehran University of Medical Sciences 2014
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4499094/
https://ncbi.nlm.nih.gov/pubmed/26171365
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