Showing 1 - 1 results of 1 for search 'Soraya Gholizad-kolveiri', query time: 0.01s Refine Results
  1. 1
    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 Soraya Gholizad-kolveiri, Nakysa Hooman, Rasoul Alizadeh, Rozita Hoseini, Hasan Otukesh, Saeed Talebi, Mansoureh Akouchekian

    Published 2020
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: