Title : Kennedy's disease (spinal and bulbar muscular atrophy): a clinically oriented review of a rare disease.

Pub. Date : 2019 Mar

PMID : 30006721






1 Functional Relationships(s)
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1 An expanded trinucleotide repeat (CAG > 37) in the androgen receptor gene (AR), encoding glutamine, is the mutation responsible for Kennedy"s disease. GUANOSINE 5'-TRIPHOSPHATE P3-[1-(2-NITROPHENYL)ETHYL ESTER] androgen receptor Homo sapiens