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April 30, 2015Pediatric Blood & Cancer

Wiskott–Aldrich syndrome/X‐linked thrombocytopenia in China: Clinical characteristic and genotype–phenotype correlation

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Authors

ZZZhiyong ZhangChildren's Hospital of Chongqing Medical UniversityQZQin ZhaoQingdao UniversityLJLiping JiangCentral South University

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Zhang et al. (2015) studied this question.

synapsesocial.com/papers/6aa498a99bfc60db011424cbhttps://doi.org/10.1002/pbc.25559
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Spontaneous In Vivo Reversion of an Inherited Mutation in the Wiskott-Aldrich Syndrome2001 · 111 citations
  2. 2X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options2010 · 217 citations
  3. 3Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation2004 · 342 citations
  4. 4Expression of Wiskott-Aldrich Syndrome Protein (WASP) Gene During Hematopoietic Differentiation1997 · 92 citations