Mutation in the gene encoding the Wiskott-Aldrich Syndrome protein (WASP) has been identified as the genetic defect responsible for WAS, an X-linked primary immunodeficiency disease characterized by eczema, thrombocytopenia, and recurrent infections. In this study, the WASP gene of 7 unrelated patie
β¦ LIBER β¦
Novel mutations, no detectable mRNA and familial genetic analysis of the Wiskott-Aldrich syndrome protein gene in six Japanese patients with Wiskott-Aldrich syndrome
β Scribed by Sasahara, Y.; Kawai, S.; Kumaki, S.; Ohashi, Y.; Minegishi, M.; Tsuchiya, S.
- Book ID
- 113042810
- Publisher
- Springer
- Year
- 2000
- Tongue
- English
- Weight
- 250 KB
- Volume
- 159
- Category
- Article
- ISSN
- 0340-6997
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