Congenital dyserythropoietic anemia type 1: a case with novel compound heterozygous mutations in the C15orf41 gene.

Palmblad, Jan; Sander, Birgitta; Bain, Barbara; Klimkowska, Monika; Björck, Erik

Palmblad, Jan; Sander, Birgitta; Bain, Barbara; Klimkowska, Monika; Björck, Erik.

Afiliación

Palmblad J; Departments of Hematology and Medicine, The Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
Sander B; Department of Laboratory Medicine, Division of Pathology, The Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
Bain B; Centre for Haematology, Imperial College London Faculty of Medicine, St Mary's Hospital, London.
Klimkowska M; Department of Laboratory Medicine, Division of Pathology, The Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
Björck E; Clinical Genetics, Department of Molecular Medicine and Surgery, The Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.

Am J Hematol ; 2018 Jun 08.

Article en En | MEDLINE | ID: mdl-29885034

Palabras clave

CDA1; neutropenia; novel mutation

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Am J Hematol Año: 2018 Tipo del documento: Article País de afiliación: Suecia

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