Title : Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease.

Pub. Date : 2019 Jan 29

PMID : 30699348






3 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Spinocerebellar ataxia type 7 (SCA7) is a retinal-cerebellar degenerative disorder caused by CAG-polyglutamine (polyQ) repeat expansions in the ataxin-7 gene. polyglutamine ataxin 7 Homo sapiens
2 Spinocerebellar ataxia type 7 (SCA7) is a retinal-cerebellar degenerative disorder caused by CAG-polyglutamine (polyQ) repeat expansions in the ataxin-7 gene. polyglutamine ataxin 7 Homo sapiens
3 Spinocerebellar ataxia type 7 (SCA7) is a retinal-cerebellar degenerative disorder caused by CAG-polyglutamine (polyQ) repeat expansions in the ataxin-7 gene. polyglutamine ataxin 7 Homo sapiens