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A novel variant DO*A allele with a c.370delT mutation leading to a DO-null phenotype in a Syrian family.
A novel variant DO*A allele with a c.370delT mutation leading to a DO-null phenotype in a Syrian family.
2020
Pierre-Aurèle Morin
Carole Éthier
Josée Lavoie
Nancy Robitaille
Nadia Baillargeon
Keywords:
null phenotype
Mutation
Biology
Allele
Genetics
Correction
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