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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| Main Authors: | , |
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| Format: | Online |
| Language: | English |
| Published: |
Universidade Estadual de Campinas
2019
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| Subjects: | |
| Online Access: | https://econtents.sbu.unicamp.br/eventos/index.php/pibic/article/view/1088 |
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