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Article

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

Haematologica - 1 Apr 2010

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

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Topics

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Share to Splenomegaly
Share to Child, Preschool
Share to Flow Cytometry
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to X-Linked Inhibitor of Apoptosis Protein

Source

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Identifiers

PMID: 20015872
DOI: 10.3324/haematol.2009.018010
PMCID: PMC2857205

Genes

XIAP

Provenance

PubMed metadata and Literature Corpus relationships.

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A novel XIAP mutation in a Japanese boy with recurrent pancytopenia and splenomegaly.PMID 20015872Read ↗

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