Title : [Dynamic mutations in hereditary neurodegenerative disorders].

Pub. Date : 1999 Aug 30

PMID : 10504853






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Short cytosine-adenine-guanine (CAG) expansions are characteristic for Huntington"s disease (HD), spinal and bulbar muscular atrophy (SBMA), dentatorubral-pallidoluysian atrophy (DRPLA) and spinocerebellar ataxia (SCA) type 1, 2, 3, 6 and 7. GUANOSINE 5'-TRIPHOSPHATE P3-[1-(2-NITROPHENYL)ETHYL ESTER] androgen receptor Homo sapiens