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7. The genotype of the original Wiskott phenotype. Binder V, Albert MH, Kabus M, Bertone M, Meindl A, Belohradsky BH. N Engl J Med; 2006 Oct 26; 355(17):1790-3. PubMed ID: 17065640 [Abstract] [Full Text] [Related]
9. Novel WASP mutation in a patient with Wiskott-Aldrich syndrome: Case report and review of the literature. Eghbali M, Sadeghi-Shabestari M, Najmi Varzaneh F, Zare Bidoki A, Rezaei N. Allergol Immunopathol (Madr); 2016 Oct 26; 44(5):450-4. PubMed ID: 26993433 [Abstract] [Full Text] [Related]
10. The Wiskott-Aldrich syndrome: The actin cytoskeleton and immune cell function. Blundell MP, Worth A, Bouma G, Thrasher AJ. Dis Markers; 2010 Oct 26; 29(3-4):157-75. PubMed ID: 21178275 [Abstract] [Full Text] [Related]
11. Clinical Manifestations and Pathophysiological Mechanisms of the Wiskott-Aldrich Syndrome. Candotti F. J Clin Immunol; 2018 Jan 26; 38(1):13-27. PubMed ID: 29086100 [Abstract] [Full Text] [Related]
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15. New insights into the biology of Wiskott-Aldrich syndrome (WAS). Thrasher AJ. Hematology Am Soc Hematol Educ Program; 2009 Aug 26; ():132-8. PubMed ID: 20008191 [Abstract] [Full Text] [Related]
16. Wiskott-Aldrich syndrome caused by a new mutation associated with multifocal dermal juvenile xanthogranulomas. Jesenak M, Plamenova I, Plank L, Banovcin P. Pediatr Dermatol; 2013 Aug 26; 30(5):e91-3. PubMed ID: 23157619 [Abstract] [Full Text] [Related]
18. A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4. Doğu F, Ariga T, Ikincioğullari A, Bozdoğan G, Aytekin C, Metin A, Babacan E. Turk J Pediatr; 2006 Aug 26; 48(1):66-8. PubMed ID: 16562789 [Abstract] [Full Text] [Related]
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20. Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia. Andreu N, Matamoros N, Escudero A, Fillat C. Int J Mol Med; 2007 May 26; 19(5):777-82. PubMed ID: 17390083 [Abstract] [Full Text] [Related] Page: [Next] [New Search]