The novel missense variant c.350G>T on the ABO*B.01 allele associated with a B<sub>el</sub> phenotype.

Kim, Tae Yeul; Yu, HongBi; Chung, Yoo Na; Jang, Ja-Hyun; Cho, Duck

The novel missense variant c.350G>T on the ABO*B.01 allele associated with a B_el phenotype.

Kim, Tae Yeul; Yu, HongBi; Chung, Yoo Na; Jang, Ja-Hyun; Cho, Duck.

Afiliação

Kim TY; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Yu H; Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul, South Korea.
Chung YN; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Jang JH; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Cho D; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

Transfusion ; 60(10): E36-E37, 2020 10.

Article em En | MEDLINE | ID: mdl-32959374

Assuntos

Sistema ABO de Grupos Sanguíneos/genética; Alelos; Mutação de Sentido Incorreto; Humanos; Masculino

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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Sistema ABO de Grupos Sanguíneos / Mutação de Sentido Incorreto / Alelos Tipo de estudo: Risk_factors_studies Limite: Humans / Male Idioma: En Revista: Transfusion Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Coréia do Sul

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