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Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion
- Source :
- Neurology. 54(12)
- Publication Year :
- 2000
-
Abstract
- Article abstract The GAA triplet repeat expansion that causes Friedreich ataxia is found only in individuals of European, North African, Middle Eastern, or Indian origin (Indo-European and Afro-Asiatic speakers). Analysis of normal alleles of the GAA repeat and of closely linked markers suggests that expansions arose through a unique two-step process. A major implication of these findings is that Friedreich ataxia may not exist among sub-Saharan Africans, Amerindians, and people from China, Japan, and Southeast Asia.
- Subjects :
- Genetic Markers
Ataxia
Asia
Genetic Linkage
Ethnic group
Black People
Biology
White People
Middle East
Africa, Northern
Asian People
Genetic linkage
Iron-Binding Proteins
Ethnic distribution
medicine
Humans
Allele
Alleles
Genetics
Triplet repeat
Haplotype
Founder Effect
Europe
Phosphotransferases (Alcohol Group Acceptor)
Haplotypes
Friedreich Ataxia
Neurology (clinical)
medicine.symptom
Trinucleotide Repeat Expansion
Founder effect
Subjects
Details
- ISSN :
- 00283878
- Volume :
- 54
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Neurology
- Accession number :
- edsair.doi.dedup.....68f8e1518ed1edffecf163a25494784e