A novel mutation F826L in the human androgen receptor in partial androgen insensitivity syndrome; increased NH2-/COOH-terminal domain interaction and TIF2 co-activation.

Source:http://linkedlifedata.com/resource/pubmed/id/18656523

Mol. Cell. Endocrinol. 2008 Sep 24 292 1-2 69-78

Download in:

View as

Triples

General Info

PMID
18656523