Title : Molecular genetics of spinocerebellar ataxia type 8 (SCA8).

Pub. Date : 2005 Apr

PMID : 17132942






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The majority of these diseases result from expanded polyglutamine tracts in the encoded protein as seen in SCA1, SCA2, SCA3, SCA6, SCA7 and Dentatorubral-Pallidoluysian Atrophy (DRPLA). polyglutamine atrophin 1 Homo sapiens