| pubmed-article:8815938 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8815938 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:8815938 | lifeskim:mentions | umls-concept:C0016719 | lld:lifeskim |
| pubmed-article:8815938 | lifeskim:mentions | umls-concept:C0262496 | lld:lifeskim |
| pubmed-article:8815938 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
| pubmed-article:8815938 | pubmed:issue | 16 | lld:pubmed |
| pubmed-article:8815938 | pubmed:dateCreated | 1997-1-23 | lld:pubmed |
| pubmed-article:8815938 | pubmed:abstractText | Friedreich's ataxia, the most common inherited ataxia, is associated with a mutation that consists of an unstable expansion of GAA repeats in the first intron of the frataxin gene on chromosome 9, which encodes a protein of unknown function. | lld:pubmed |
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| pubmed-article:8815938 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8815938 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8815938 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:8815938 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8815938 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:8815938 | pubmed:issn | 0028-4793 | lld:pubmed |
| pubmed-article:8815938 | pubmed:author | pubmed-author:AgidYY | lld:pubmed |
| pubmed-article:8815938 | pubmed:author | pubmed-author:MandelJ LJL | lld:pubmed |
| pubmed-article:8815938 | pubmed:author | pubmed-author:KoenigMM | lld:pubmed |
| pubmed-article:8815938 | pubmed:author | pubmed-author:PenetCC | lld:pubmed |
| pubmed-article:8815938 | pubmed:author | pubmed-author:DürrAA | lld:pubmed |
| pubmed-article:8815938 | pubmed:author | pubmed-author:BriceAA | lld:pubmed |
| pubmed-article:8815938 | pubmed:author | pubmed-author:CampuzanoVV | lld:pubmed |
| pubmed-article:8815938 | pubmed:author | pubmed-author:MignardCC | lld:pubmed |
| pubmed-article:8815938 | pubmed:author | pubmed-author:CosseeMM | lld:pubmed |
| pubmed-article:8815938 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8815938 | pubmed:day | 17 | lld:pubmed |
| pubmed-article:8815938 | pubmed:volume | 335 | lld:pubmed |
| pubmed-article:8815938 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8815938 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8815938 | pubmed:pagination | 1169-75 | lld:pubmed |
| pubmed-article:8815938 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:8815938 | pubmed:year | 1996 | lld:pubmed |
| pubmed-article:8815938 | pubmed:articleTitle | Clinical and genetic abnormalities in patients with Friedreich's ataxia. | lld:pubmed |
| pubmed-article:8815938 | pubmed:affiliation | Fédération de Neurologie and INSERM Unité 289, Hôpital de la Saltpétriere, Paris, France. | lld:pubmed |
| pubmed-article:8815938 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8815938 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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