| pubmed-article:11723290 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11723290 | lifeskim:mentions | umls-concept:C0007758 | lld:lifeskim |
| pubmed-article:11723290 | lifeskim:mentions | umls-concept:C0443147 | lld:lifeskim |
| pubmed-article:11723290 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:11723290 | pubmed:dateCreated | 2001-11-27 | lld:pubmed |
| pubmed-article:11723290 | pubmed:abstractText | A kindred is described with a dominantly inherited "pure" cerebellar ataxia in which the currently known spinocerebellar ataxias have been excluded. In the eight subjects studied, a notable clinical feature is slow progression, with the three least affected having only a mild degree of gait ataxia after three or more decades of disease duration. Pending an actual chromosomal locus discovery, the name spinocerebellar ataxia (SCA)15 is expectantly applied. | lld:pubmed |
| pubmed-article:11723290 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11723290 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11723290 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:11723290 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11723290 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:11723290 | pubmed:issn | 0028-3878 | lld:pubmed |
| pubmed-article:11723290 | pubmed:author | pubmed-author:GardnerR JRJ | lld:pubmed |
| pubmed-article:11723290 | pubmed:author | pubmed-author:NicholsonG... | lld:pubmed |
| pubmed-article:11723290 | pubmed:author | pubmed-author:StoreyEE | lld:pubmed |
| pubmed-article:11723290 | pubmed:author | pubmed-author:TuckR RRR | lld:pubmed |
| pubmed-article:11723290 | pubmed:author | pubmed-author:KnightM AMA | lld:pubmed |
| pubmed-article:11723290 | pubmed:author | pubmed-author:ForrestS MSM | lld:pubmed |
| pubmed-article:11723290 | pubmed:author | pubmed-author:KennersonM... | lld:pubmed |
| pubmed-article:11723290 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11723290 | pubmed:day | 27 | lld:pubmed |
| pubmed-article:11723290 | pubmed:volume | 57 | lld:pubmed |
| pubmed-article:11723290 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11723290 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11723290 | pubmed:pagination | 1913-5 | lld:pubmed |
| pubmed-article:11723290 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:11723290 | pubmed:meshHeading | pubmed-meshheading:11723290... | lld:pubmed |
| pubmed-article:11723290 | pubmed:meshHeading | pubmed-meshheading:11723290... | lld:pubmed |
| pubmed-article:11723290 | pubmed:meshHeading | pubmed-meshheading:11723290... | lld:pubmed |
| pubmed-article:11723290 | pubmed:meshHeading | pubmed-meshheading:11723290... | lld:pubmed |
| pubmed-article:11723290 | pubmed:meshHeading | pubmed-meshheading:11723290... | lld:pubmed |
| pubmed-article:11723290 | pubmed:meshHeading | pubmed-meshheading:11723290... | lld:pubmed |
| pubmed-article:11723290 | pubmed:meshHeading | pubmed-meshheading:11723290... | lld:pubmed |
| pubmed-article:11723290 | pubmed:year | 2001 | lld:pubmed |
| pubmed-article:11723290 | pubmed:articleTitle | A new autosomal dominant pure cerebellar ataxia. | lld:pubmed |
| pubmed-article:11723290 | pubmed:affiliation | Genetic Health Services Victoria at the Alfred Hospital, Monash University, Alfred Hospital, Parkville, Melbourne, Australia. | lld:pubmed |
| pubmed-article:11723290 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11723290 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:3708 | entrezgene:pubmed | pubmed-article:11723290 | lld:entrezgene |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11723290 | lld:pubmed |
