| pubmed-article:9484389 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9484389 | lifeskim:mentions | umls-concept:C1514805 | lld:lifeskim |
| pubmed-article:9484389 | lifeskim:mentions | umls-concept:C0014550 | lld:lifeskim |
| pubmed-article:9484389 | lifeskim:mentions | umls-concept:C0012929 | lld:lifeskim |
| pubmed-article:9484389 | lifeskim:mentions | umls-concept:C1442161 | lld:lifeskim |
| pubmed-article:9484389 | lifeskim:mentions | umls-concept:C0439064 | lld:lifeskim |
| pubmed-article:9484389 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:9484389 | pubmed:dateCreated | 1998-3-16 | lld:pubmed |
| pubmed-article:9484389 | pubmed:abstractText | In a patient with clinical features of myoclonus epilepsy with ragged red fibers (MERRF), molecular genetic analysis of mitochondrial DNA did not show either of the two point mutations typically associated with MERRF but did show multiple deletions by Southern blot. This case further illustrates the heterogeneity observed with mtDNA mutations. | lld:pubmed |
| pubmed-article:9484389 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9484389 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9484389 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9484389 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:9484389 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9484389 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9484389 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9484389 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9484389 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9484389 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9484389 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9484389 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:9484389 | pubmed:issn | 0028-3878 | lld:pubmed |
| pubmed-article:9484389 | pubmed:author | pubmed-author:DiMauroSS | lld:pubmed |
| pubmed-article:9484389 | pubmed:author | pubmed-author:BodensteinerJ... | lld:pubmed |
| pubmed-article:9484389 | pubmed:author | pubmed-author:SchochetS SSS | lld:pubmed |
| pubmed-article:9484389 | pubmed:author | pubmed-author:ShanskeSS | lld:pubmed |
| pubmed-article:9484389 | pubmed:author | pubmed-author:SantorelliF... | lld:pubmed |
| pubmed-article:9484389 | pubmed:author | pubmed-author:BlumenthalD... | lld:pubmed |
| pubmed-article:9484389 | pubmed:author | pubmed-author:JaynesmMM | lld:pubmed |
| pubmed-article:9484389 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9484389 | pubmed:volume | 50 | lld:pubmed |
| pubmed-article:9484389 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9484389 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9484389 | pubmed:pagination | 524-5 | lld:pubmed |
| pubmed-article:9484389 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:meshHeading | pubmed-meshheading:9484389-... | lld:pubmed |
| pubmed-article:9484389 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9484389 | pubmed:articleTitle | Myoclonus epilepsy with ragged red fibers and multiple mtDNA deletions. | lld:pubmed |
| pubmed-article:9484389 | pubmed:affiliation | Department of Neurology, West Virginia University Hospitals, Morgantown, USA. | lld:pubmed |
| pubmed-article:9484389 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9484389 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:9484389 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:9484389 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9484389 | lld:pubmed |
