Hasil Pencarian - Mohammad Hossein Taskhiri

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  1. 1
    A Heterozygous STXBP1 Gene de novo Mutation in an Iranian Child With Epileptic Encephalopathy: Case Report

    A Heterozygous STXBP1 Gene de novo Mutation in an Iranian Child With Epileptic Encephalopathy: Case Report oleh Masoud Heidari, Morteza Soleyman-Nejad, Mohammad Hossein Taskhiri, Alireza Isazadeh, Manzar Bolhassan, Javad Shahpouri, Mansour Heidari, Nahid Sadighi

    Diterbitkan 2020-02-01
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  2. 2
    Association of a novel homozygous mutation in the HMGCS2 gene with an HMGCSD in an Iranian patient

    Association of a novel homozygous mutation in the HMGCS2 gene with an HMGCSD in an Iranian patient oleh Masoud Heidari, Morteza Soleyman‐Nejad, Alireza Isazadeh, Javad Shapouri, Mohammad Hossein Taskhiri, Roghayyeh Ahangari, Ali Reza Mohamadi, Masoumeh Ebrahimi, Hadi Karimi, Manzar Bolhassani, Zahra Karimi, Mansour Heidari

    Diterbitkan 2020-11-01
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