Deletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity in this syndrome.

The cloning of a cDNA for the human androgen receptor gene has resulted in the availability of cDNA probes that span various parts of the gene, including the entire steroid-binding domain and part of the DNA-binding domain, as well as part of the 5' region of the gene. The radiolabeled probes w...

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Bibliografiska uppgifter
I publikationen:Proc Natl Acad Sci U S A
Huvudupphovsmän: Brown, T R, Lubahn, D B, Wilson, E M, Joseph, D R, French, F S, Migeon, C J
Materialtyp: Artigo
Språk:Inglês
Publicerad: National Academy of Sciences 1988
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC282385/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3186717/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.85.21.8151
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