Rare P<sup>k</sup> phenotype caused by a novel frameshift mutation in B3GALNT1.

Ma, Ling; Wang, Enbo; Liu, Taixiang; Huang, Chengyin; Ding, Wenyi

Rare P^k phenotype caused by a novel frameshift mutation in B3GALNT1.

Ma, Ling; Wang, Enbo; Liu, Taixiang; Huang, Chengyin; Ding, Wenyi.

Afiliación

Ma L; Department of Transfusion Research, Jiangsu Province Blood Center, Nanjing, China.
Wang E; Department of Transfusion Medicine, The First People's Hospital of Lianyungang, Lianyungang, China.
Liu T; Department of Transfusion Research, Jiangsu Province Blood Center, Nanjing, China.
Huang C; Department of Transfusion Research, Jiangsu Province Blood Center, Nanjing, China.
Ding W; Department of Transfusion Research, Jiangsu Province Blood Center, Nanjing, China.

Transfus Med ; 33(2): 179-180, 2023 04.

Article en En | MEDLINE | ID: mdl-35836312

Asunto(s)

Mutación del Sistema de Lectura; Humanos; Fenotipo

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Mutación del Sistema de Lectura Límite: Humans Idioma: En Revista: Transfus Med Asunto de la revista: HEMATOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: China

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