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Clinical and Molecular Analysis of Children with Wiskott-Aldrich Syndrome to indicate Bone Marrow Transplantation

Wiskott-Aldrich Syndrome (WAS) is a genetic disease linked to the X chromosome, characterized by recurrent infections, autoimmunity, malignancy, eczema and hemorrhage. Mutations in the WAS gene alter the coding of the WASp protein, expressed mainly in the cytoplasm of hematopoietic cells, with funct...

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Bibliographic Details
Main Authors:	Cardim, Nathalie, Vilela, Maria Marluce dos Santos
Format:	Online
Language:	English
Published:	Universidade Estadual de Campinas 2019
Subjects:	Wiskott-Aldrich syndrome Phenotype Bone marrow transplant.
Online Access:	https://econtents.sbu.unicamp.br/eventos/index.php/pibic/article/view/1088
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