A novel XIAP mutation in a Japanese boy with recurrent pancytopenia and splenomegaly.

Zhao, Meina; Kanegane, Hirokazu; Ouchi, Kazutaka; Imamura, Toshihiko; Latour, Sylvain; Miyawaki, Toshio

Zhao, Meina; Kanegane, Hirokazu; Ouchi, Kazutaka; Imamura, Toshihiko; Latour, Sylvain; Miyawaki, Toshio.

Haematologica ; 95(4): 688-9, 2010 Apr.

Article in En | MEDLINE | ID: mdl-20015872

Subject(s)

Mutation/genetics; Pancytopenia/genetics; Splenomegaly/genetics; X-Linked Inhibitor of Apoptosis Protein/genetics; Child, Preschool; Female; Flow Cytometry; Humans; Lymphocytes/metabolism; Lymphocytes/pathology; Male; Mothers; Recurrence; Splenomegaly/pathology

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancytopenia / Splenomegaly / X-Linked Inhibitor of Apoptosis Protein / Mutation Limits: Child, preschool / Female / Humans / Male Language: En Journal: Haematologica Year: 2010 Document type: Article Country of publication: Italy

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