Search Results - Mehrtash, Amir Hosein

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    Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII

    Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII by Ebrahimi, Amir Hossein, Bolhassani, Manzar, Zarei, Mohammad Reza, Heidari, Matin, ArdeshirDavani, Amin, Mehrtash, Amir Hosein, Shiri, Zahra, Heidari, Masoud, Soleyman-Nejad, Morteza, Taskhiri, Mohammad Hossein, Norouzbeigi, Arefeh, Heidari, Mansour

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