Pub. Date : 1999 Jul
PMID : 10369863
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Spinocerebellar ataxia type 6 (SCA6) is one of the eight neurodegenerative diseases caused by a tri-nucleotide (CAG) repeat expansion coding polyglutamine (CAG repeat/polyglutamine diseases) and is characterized by late onset autosomal dominant cerebellar ataxia and predominant loss of cerebellar Purkinje cells. | tri-nucleotide | calcium voltage-gated channel subunit alpha1 A | Homo sapiens |
2 | Spinocerebellar ataxia type 6 (SCA6) is one of the eight neurodegenerative diseases caused by a tri-nucleotide (CAG) repeat expansion coding polyglutamine (CAG repeat/polyglutamine diseases) and is characterized by late onset autosomal dominant cerebellar ataxia and predominant loss of cerebellar Purkinje cells. | tri-nucleotide | calcium voltage-gated channel subunit alpha1 A | Homo sapiens |