- A Case of Wiskott-Aldrich Syndrome with 1316 G Deletion in Exon 10 on X-chromosome Treated with Allogeneic Cord Blood Transplantation
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Kwon DG, Lee KG, Jee YH, Chung HJ, Baatartsoget O, Choi KD, Park JE
- KMID: 2279920
- Clin Pediatr Hematol Oncol.
- 2007 Oct;14(2):207-211.
Wiskott-Aldrich syndrome, an X-linked immuno-deficiency disorder caused by mutations of Wiskott-Aldrich syndrome protein (WASP) gene, is characterized by thrombocytopenia, recurrent infections, and eczema. Most of the cases of Wiskott-Aldrich syndrome,... -
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