Severe combined immune deficiency due to a homozygous 3.2-kb deletion spanning the promoter and first exon of the adenosine deaminase gene.

We have investigated the structural gene for adenosine deaminase (ADA) in a female infant with ADA deficiency associated severe combined immune deficiency (ADA-SCID) disease and her family by DNA restriction-fragment-length analysis. In this family a new ADA-specific restriction-fragment-length vari...

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書目詳細資料

發表在:	Nucleic Acids Res
Principais autores:	Berkvens, T M, Gerritsen, E J, Oldenburg, M, Breukel, C, Wijnen, J T, van Ormondt, H, Vossen, J M, van der Eb, A J, Meera Khan, P
格式:	Artigo
語言:	Inglês
出版:	Oxford University Press 1987
在線閱讀:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC306474/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3684597/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/15.22.9365
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