Title : Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody.

Pub. Date : 1999 Dec 10

PMID : 10640674






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The spinocerebellar ataxia type 7 (SCA7) is associated with pigmentary macular dystrophy and retinal degeneration leading to blindness caused by a CAG/polyglutamine (polyGln) expansion in the coding region of the SCA7 gene/protein. polyglutamine ataxin 7 Homo sapiens
2 The spinocerebellar ataxia type 7 (SCA7) is associated with pigmentary macular dystrophy and retinal degeneration leading to blindness caused by a CAG/polyglutamine (polyGln) expansion in the coding region of the SCA7 gene/protein. polyglutamine ataxin 7 Homo sapiens