Search Results - "Abhari, Masoumeh"

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    Mutation analysis of familial GJB2-related deafness in Iranian Azeri Turkish patients by Bonyadi, Mortaza, Esmaeili, Mohsen, Abhari, Masoumeh, Lotfi, Alireza

    Published in Genetic testing and molecular biomarkers (01-10-2009)
    “…Mutations in the GJB2 gene-encoding connexin 26 protein are the main cause for autosomal recessive nonsyndromic hearing loss worldwide. In this study, we…”
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    Journal Article