Whole Wiskott-Aldrich syndrome protein gene deletion identified by high throughput sequencing

Wiskott-Aldrich syndrome (WAS) is a rare X-linked recessive immunodeficiency disorder, characterized by thrombocytopenia, small platelets, eczema and recurrent infections associated with increased risk of autoimmunity and malignancy disorders. Mutations in the WAS protein (WASP) gene are responsible...

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Detalles Bibliográficos
Autores principales: He, Xiangling, Zou, Runying, Zhang, Bing, You, Yalan, Yang, Yang, Tian, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865821/
https://www.ncbi.nlm.nih.gov/pubmed/28901403
http://dx.doi.org/10.3892/mmr.2017.7416

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865821/
https://www.ncbi.nlm.nih.gov/pubmed/28901403
http://dx.doi.org/10.3892/mmr.2017.7416

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