Title : Mutant ataxin1 disrupts cerebellar development in spinocerebellar ataxia type 1.

Pub. Date : 2018 Jun 1

PMID : 29533923






3 Functional Relationships(s)
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Protein Name
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1 Spinocerebellar ataxia type 1 (SCA1) is an adult-onset neurodegenerative disease caused by a polyglutamine expansion in the protein ATXN1, which is involved in transcriptional regulation. polyglutamine ataxin 1 Homo sapiens
2 Spinocerebellar ataxia type 1 (SCA1) is an adult-onset neurodegenerative disease caused by a polyglutamine expansion in the protein ATXN1, which is involved in transcriptional regulation. polyglutamine ataxin 1 Homo sapiens
3 Spinocerebellar ataxia type 1 (SCA1) is an adult-onset neurodegenerative disease caused by a polyglutamine expansion in the protein ATXN1, which is involved in transcriptional regulation. polyglutamine ataxin 1 Homo sapiens