Title : Spinocerebellar ataxia type 7 (SCA7): widespread brain damage in an adult-onset patient with progressive visual impairments in comparison with an adult-onset patient without visual impairments.

Pub. Date : 2008 Apr

PMID : 17971076






2 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Spinocerebellar ataxia type 7 (SCA7) represents a rare and severe autosomal dominantly inherited ataxic disorder and is among the known CAG-repeat, or polyglutamine, diseases. polyglutamine ataxin 7 Homo sapiens
2 Spinocerebellar ataxia type 7 (SCA7) represents a rare and severe autosomal dominantly inherited ataxic disorder and is among the known CAG-repeat, or polyglutamine, diseases. polyglutamine ataxin 7 Homo sapiens