Patient diagnosed with Wiskott Aldrich and presence of a new mutation

Article

Abstract: Introduction: Wiskott Aldrich syndrome is a primary immunodeficiency, rarely inherited in a recessiv

Palabras claves:

mutation, Purple, thrombocytopenia, Wiskott Aldrich syndrome, Wiskott Aldrich syndrome protein, X chromosome

Autores:

Cedeño Velez L.F., Eduardo Josué Milian-Hernández, Jazmín Beatríz Anzules Guerra, Zevallos I.V.

Fuentes:

scopus