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

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

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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, (Summary Text)

Publication Type: Conference Paper / Summary Text
City: BARSELONA
Country: Spain
Karadeniz Technical University Affiliated: No