Title : Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase.

Pub. Date : 1996 Sep

PMID : 8872471






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Spinocerebellar ataxia type1 (SCA1) is one of several neurodegenerative disorders caused by expansions of translated CAG trinucleotide repeats which code for polyglutamine in the respective proteins. polyglutamine ataxin 1 Homo sapiens
2 Spinocerebellar ataxia type1 (SCA1) is one of several neurodegenerative disorders caused by expansions of translated CAG trinucleotide repeats which code for polyglutamine in the respective proteins. polyglutamine ataxin 1 Homo sapiens