Title : Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy.

Pub. Date : 2004 Jan

PMID : 14571264






4 Functional Relationships(s)
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1 The disease is caused by expansion of a CAG trinucleotide repeat within the SCA7 gene, which encodes a polyglutamine tract within a novel protein, termed ataxin-7. polyglutamine ataxin 7 Homo sapiens
2 The disease is caused by expansion of a CAG trinucleotide repeat within the SCA7 gene, which encodes a polyglutamine tract within a novel protein, termed ataxin-7. polyglutamine ataxin 7 Homo sapiens
3 The expansion of polyglutamine-encoding CAG repeats in dissimilar genes underlies eight neurodegenerative conditions besides SCA7, including a number of dominant ataxias related to SCA7. polyglutamine ataxin 7 Homo sapiens
4 The expansion of polyglutamine-encoding CAG repeats in dissimilar genes underlies eight neurodegenerative conditions besides SCA7, including a number of dominant ataxias related to SCA7. polyglutamine ataxin 7 Homo sapiens