Title : Two populations of neuronal intranuclear inclusions in SCA7 differ in size and promyelocytic leukaemia protein content.

Pub. Date : 2002 Jul

PMID : 12077003






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Spinocerebellar ataxia type 7 (SCA7) is a hereditary progressive cerebellar ataxia with retinal degeneration associated with an abnormally expanded polyglutamine stretch. polyglutamine ataxin 7 Homo sapiens
2 Spinocerebellar ataxia type 7 (SCA7) is a hereditary progressive cerebellar ataxia with retinal degeneration associated with an abnormally expanded polyglutamine stretch. polyglutamine ataxin 7 Homo sapiens