A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B<sub>w</sub> phenotype.

Hult, Annika K; Hellberg, Åsa; Storry, Jill R; Písacka, Martin; Olsson, Martin L

A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B_w phenotype.

Hult, Annika K; Hellberg, Åsa; Storry, Jill R; Písacka, Martin; Olsson, Martin L.

Afiliación

Hult AK; Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Hellberg Å; Department of Clinical Immunology and Transfusion Medicine, Office for Medical Services, Lund, Sweden.
Storry JR; Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Písacka M; Department of Clinical Immunology and Transfusion Medicine, Office for Medical Services, Lund, Sweden.
Olsson ML; Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden.

Transfusion ; 62(10): E55-E58, 2022 10.

Article en En | MEDLINE | ID: mdl-36125051

Asunto(s)

Sistema del Grupo Sanguíneo ABO; Mutación Missense; Sistema del Grupo Sanguíneo ABO/genética; Alelos; Exones/genética; Genotipo; Fenotipo

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sistema del Grupo Sanguíneo ABO / Mutación Missense Idioma: En Revista: Transfusion Año: 2022 Tipo del documento: Article País de afiliación: Suecia

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