Search Results - Gholizad-kolveiri, Soraya

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    Whole exome sequencing revealed a novel homozygous variant in the DGKE catalytic domain: a case report of familial hemolytic uremic syndrome

    Whole exome sequencing revealed a novel homozygous variant in the DGKE catalytic domain: a case report of familial hemolytic uremic syndrome by Gholizad-kolveiri, Soraya, Hooman, Nakysa, Alizadeh, Rasoul, Hoseini, Rozita, Otukesh, Hasan, Talebi, Saeed, Akouchekian, Mansoureh

    Published in BMC medical genetics
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