Maternal onset de novo SH2D1A mutation and lymphocytic choriomeningitis virus infection in a patient with X-linked lymphoproliferative disease type 1: A case report

X-linked lymphoproliferative disease type 1 (XLP1) is a rare genetic immunodeficiency disease, which occurs due to germline mutations in the SH2D1A gene. This gene has been reported to encode the adaptor molecule signaling lymphocytic activation molecule-associated protein XLP1 is generally triggere...

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Detalles Bibliográficos
Autores principales: LIU, JINRONG, TIAN, WENJUN, WANG, FANG, TENG, WEN, ZHANG, YANG, TONG, CHUNRONG, ZHANG, CHONGLIN, JU, YING, ZHANG, BINGCHANG, ZHAO, SHUNYING, LIU, HONGXING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368086/
https://www.ncbi.nlm.nih.gov/pubmed/25572984
http://dx.doi.org/10.3892/mmr.2015.3173

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368086/
https://www.ncbi.nlm.nih.gov/pubmed/25572984
http://dx.doi.org/10.3892/mmr.2015.3173

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