X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic

X-linked lymphoproliferative syndrome (XLP) is a rare primary immunodeficiency disease that can be divided into two types: SAP deficiency (XLP1) and XIAP deficiency (XLP2), caused by mutations in the SH2D1A and XIAP genes, respectively. Few cases of XLP (particularly XIAP deficiency) have been repor...

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Detalles Bibliográficos
Autores principales: Xu, Tao, Zhao, Qin, Li, Wenyan, Chen, Xuemei, Xue, Xiuhong, Chen, Zhi, Du, Xiao, Bai, Xiaoming, Zhao, Qian, Zhou, Lina, Tang, Xuemei, Yang, Xi, Kanegane, Hirokazu, Zhao, Xiaodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970958/
https://www.ncbi.nlm.nih.gov/pubmed/31754776
http://dx.doi.org/10.1007/s00431-019-03512-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970958/
https://www.ncbi.nlm.nih.gov/pubmed/31754776
http://dx.doi.org/10.1007/s00431-019-03512-7

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