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.

Affiliation

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 de En | MEDLINE | ID: mdl-35836312

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Mutation avec décalage du cadre de lecture Limites: Humans Langue: En Journal: Transfus Med Sujet du journal: HEMATOLOGIA Année: 2023 Type de document: Article Pays d'affiliation: Chine

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