A case wit mitochondrial seryl-tRNA synthease (SARS2) DEFECT: a novel mutation and a different phenotype from HUPRA syndrome | AVESİS

Karadeniz Technical University Research Information System

A case wit mitochondrial seryl-tRNA synthease (SARS2) DEFECT: a novel mutation and a different phenotype from HUPRA syndrome

HİŞMİ B., BELOSTOTSKY R., UTİNE G. E. , TALİM B., ÜNAL Ö., DURSUN A., ...More

12nd International Congress of Inborn Errors of Metabolism, BARSELONA, Spain, 3 - 06 September 2013

Publication Type: Conference Paper / Summary Text
City: BARSELONA
Country: Spain