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A novelWASPgene mutation in a Chinese boy with Wiskott–Aldrich syndrome

✍ Scribed by Hongtao Yu; Ting Liu; Wentong Meng; Li Hou


Book ID
107619094
Publisher
Carden Jennings Publishing
Year
2010
Tongue
English
Weight
263 KB
Volume
92
Category
Article
ISSN
0925-5710

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The Wiskott-Aldrich Syndrome (WAS) is an X-linked recessive immunodeficiency caused by mutation in the gene encoding WAS protein (WASP). The disease is characterized by eczema, thrombocytopenia and severe immunodeificency and is associated with extensive clinical heterogeneity. Mutation studies indi