Ontology highlight
ABSTRACT:
SUBMITTER: Lee KK
PROVIDER: S-EPMC2657900 | biostudies-other | 2009
REPOSITORIES: biostudies-other
Lee Kenneth K KK Swanson Selene K SK Florens Laurence L Washburn Michael P MP Workman Jerry L JL
Epigenetics & chromatin 20090218 1
Spinocerebellar ataxia (SCA) is a physically devastating, genetically inherited disorder characterized by abnormal brain function that results in the progressive loss of the ability to coordinate movements. There are many types of SCAs as there are various gene mutations that can cause this disease. SCA types 1-3, 6-10, 12, and 17 result from a trinucleotide repeat expansion in the DNA-coding sequence. Intriguingly, recent work has demonstrated that increased trinucleotde expansions in the SCA7 ...[more]