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BackgroundWiskott–Aldrich syndrome (WAS) and X‐linked thrombocytopenia (XLT) are caused by mutations of the WAS gene. The genotype–phenotype association of WAS and XLT have not been fully elucidated. Here, we established the largest database of WAS in China to further determine the potential correlation between genotype and phenotype and long‐term outcome.
ProceduresWe collected clinical data of...
To cite this article: Zhang Z‐Y, Zhao X‐D, Jiang L‐P, Liu E‐M, Cui Y‐X, Wang M, Wei H, Yu J, An Y‐F, Yang X‐Q. Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. Pediatr Allergy Immunol 2011; 22: 482–487.
AbstractOmenn syndrome (OS) is a rare autosomal recessive genetic disorder and presents symptoms of severe combined immunodeficiency characterized by...
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