X-linked SCID with a rare mutation

BACKGROUND: Severe combined immunodeficiency (SCID) is a group of relatively rare primary immunodeficiency disorders (PIDs), characterized by disturbed development of T cells and B cells, caused by several genetic mutations that bring on different clinical presentations. SCID may be inherited as an...

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Detalles Bibliográficos
Autores principales: Mahdavi, Fatemeh Sadat, Keramatipour, Mohammad, Ansari, Sarina, Sharafian, Samin, Karamzade, Arezou, Tavakol, Marzieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507167/
https://www.ncbi.nlm.nih.gov/pubmed/34635152
http://dx.doi.org/10.1186/s13223-021-00605-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507167/
https://www.ncbi.nlm.nih.gov/pubmed/34635152
http://dx.doi.org/10.1186/s13223-021-00605-7

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