An exonic point mutation creates a MaeIII site in the androgen receptor gene of a family with complete androgen insensitivity syndrome.

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Citation

Lobaccaro JM, Lumbroso S, Ktari R, Dumas R, Sultan C

An exonic point mutation creates a MaeIII site in the androgen receptor gene of a family with complete androgen insensitivity syndrome.

Hum Mol Genet. 1993 Jul;2(7):1041-3.

PubMed ID
8103398 [ View in PubMed
]
Abstract

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DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Androgen receptorP10275Details