Hasil Pencarian - Elmira Aghazadeh

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    TJP2 Gene Mutation c.G1012A May Responsible for Congenital Hearing Loss with Incomplete Penetrance in An Iranian Pedigree

    TJP2 Gene Mutation c.G1012A May Responsible for Congenital Hearing Loss with Incomplete Penetrance in An Iranian Pedigree oleh Sadegh Rajabi, Romina Dastmalchi, Mohammad Hossein Dehghan, Ali Eftekharian, Elmira Aghazadeh, Sayyed Mohammad Hossein Ghaderian

    Diterbitkan 2019-07-01
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