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Genetics of SCID

Human SCID (Severe Combined Immunodeficiency) is a prenatal disorder of T lymphocyte development, that depends on the expression of numerous genes. The knowledge of the genetic basis of SCID is essential for diagnosis (e.g., clinical phenotype, lymphocyte profile) and treatment (e.g., use and type o...

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Detalles Bibliográficos
Autor principal: Cossu, Fausto
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2999594/
https://www.ncbi.nlm.nih.gov/pubmed/21078154
http://dx.doi.org/10.1186/1824-7288-36-76