학술논문
Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.
Document Type
Article
Author
Source
Human Molecular Genetics; Feb98, Vol. 7 Issue 2, p177, 10p
Subject
Language
ISSN
09646906
Abstract
Analyzes autosomal dominant cerebellar ataxia with retinal degeneration caused by CAG triplet repeat expansion. Complications associated with the disease; Production of elongated polyglutamine tract in the corresponding protein; Correlation between the number of repeats and onset stage and the appearance of symptoms.