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Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. (3):158-160
Wiskott-Aldrich syndrome (WAS) is one of the primary immunodeficiency diseases, that is inherited as an X-linked recessive trait. Since the responsible gene, the WASP gene, has been identified, various mutations for patients with WAS have been report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc450a551f2bde45bb06f419994e5778
