| pubmed-article:9489534 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9489534 | lifeskim:mentions | umls-concept:C0439660 | lld:lifeskim |
| pubmed-article:9489534 | lifeskim:mentions | umls-concept:C0026846 | lld:lifeskim |
| pubmed-article:9489534 | lifeskim:mentions | umls-concept:C1140618 | lld:lifeskim |
| pubmed-article:9489534 | lifeskim:mentions | umls-concept:C0205108 | lld:lifeskim |
| pubmed-article:9489534 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:9489534 | pubmed:dateCreated | 1998-3-24 | lld:pubmed |
| pubmed-article:9489534 | pubmed:abstractText | To identify the clinical, electrophysiological, and genetic characteristics of a family with an unusual form of hereditary motor neuron disease. | lld:pubmed |
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| pubmed-article:9489534 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9489534 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9489534 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9489534 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9489534 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:9489534 | pubmed:issn | 0022-3050 | lld:pubmed |
| pubmed-article:9489534 | pubmed:author | pubmed-author:RajputA HAH | lld:pubmed |
| pubmed-article:9489534 | pubmed:author | pubmed-author:YeungMM | lld:pubmed |
| pubmed-article:9489534 | pubmed:author | pubmed-author:GrossD WDW | lld:pubmed |
| pubmed-article:9489534 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9489534 | pubmed:volume | 64 | lld:pubmed |
| pubmed-article:9489534 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9489534 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9489534 | pubmed:pagination | 217-20 | lld:pubmed |
| pubmed-article:9489534 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:meshHeading | pubmed-meshheading:9489534-... | lld:pubmed |
| pubmed-article:9489534 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9489534 | pubmed:articleTitle | Distal hereditary upper limb muscular atrophy. | lld:pubmed |
| pubmed-article:9489534 | pubmed:affiliation | University of Saskatchewan, Saskatoon, Canada. | lld:pubmed |
| pubmed-article:9489534 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9489534 | pubmed:publicationType | Case Reports | lld:pubmed |
