Premium
A novel variant DO*A allele with a c.370delT mutation leading to a DO ‐null phenotype in a Syrian family
Author(s) -
Morin PierreAurèle,
Ethier Carole,
Lavoie Josée,
Robitaille Nancy,
Baillargeon Nadia
Publication year - 2021
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1111/trf.16193
Subject(s) - phenotype , allele , mutation , genetics , biology , gene