Title : Molecular and electrophysiological features of spinocerebellar ataxia type seven in induced pluripotent stem cells.

Pub. Date : 2021

PMID : 33626063






3 Functional Relationships(s)
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1 Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disease caused by a polyglutamine repeat expansion in the ATXN7 gene. polyglutamine ataxin 7 Homo sapiens
2 Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disease caused by a polyglutamine repeat expansion in the ATXN7 gene. polyglutamine ataxin 7 Homo sapiens
3 Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disease caused by a polyglutamine repeat expansion in the ATXN7 gene. polyglutamine ataxin 7 Homo sapiens