@article{
 title = {Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion},
 type = {article},
 year = {2000},
 identifiers = {[object Object]},
 keywords = {Africa, Northern,Alleles,Asia,Caucasoid Race/genetics,Europe,Founder Effect,Friedreich Ataxia/*ethnology/*genetics,Genetic Markers,Haplotypes,Linkage (Genetics),Middle East,Mongoloid Race/genetics,Negroid Race/genetics,Phosphotransferases (Alcohol Group Acceptor)/genet,Support, Non-U.S. Gov't,Support, U.S. Gov't, P.H.S.,Trinucleotide Repeat Expansion/*genetics},
 pages = {2322-4.},
 volume = {54},
 id = {5299f87a-7768-396d-8ed8-bb9f69d6cfb1},
 created = {2017-06-19T13:42:59.384Z},
 file_attached = {true},
 profile_id = {de68dde1-2ff3-3a4e-a214-ef424d0c7646},
 group_id = {b2078731-0913-33b9-8902-a53629a24e83},
 last_modified = {2017-06-19T13:42:59.530Z},
 tags = {02/02/06},
 read = {false},
 starred = {false},
 authored = {false},
 confirmed = {true},
 hidden = {false},
 source_type = {Journal Article},
 notes = {<m:note>eng<m:linebreak/>Journal Article</m:note>},
 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.},
 bibtype = {article},
 author = {Labuda, M and Labuda, D and Miranda, C and Poirier, J and Soong, B W and Barucha, N E and Pandolfo, M},
 journal = {Neurology},
 number = {12}
}

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