APA (7th ed.) Citation

Soraya Gholizad-kolveiri, Nakysa Hooman, Rasoul Alizadeh, Rozita Hoseini, Hasan Otukesh, Saeed Talebi, & Mansoureh Akouchekian. (2020). Whole exome sequencing revealed a novel homozygous variant in the DGKE catalytic domain: A case report of familial hemolytic uremic syndrome. BMC.

Chicago Style (17th ed.) Citation

Soraya Gholizad-kolveiri, Nakysa Hooman, Rasoul Alizadeh, Rozita Hoseini, Hasan Otukesh, Saeed Talebi, and Mansoureh Akouchekian. Whole Exome Sequencing Revealed a Novel Homozygous Variant in the DGKE Catalytic Domain: A Case Report of Familial Hemolytic Uremic Syndrome. BMC, 2020.

MLA (9th ed.) Citation

Soraya Gholizad-kolveiri, et al. Whole Exome Sequencing Revealed a Novel Homozygous Variant in the DGKE Catalytic Domain: A Case Report of Familial Hemolytic Uremic Syndrome. BMC, 2020.