pubmed-article:18036232 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18036232 | lifeskim:mentions | umls-concept:C2700615 | lld:lifeskim |
pubmed-article:18036232 | lifeskim:mentions | umls-concept:C0032659 | lld:lifeskim |
pubmed-article:18036232 | lifeskim:mentions | umls-concept:C0425358 | lld:lifeskim |
pubmed-article:18036232 | lifeskim:mentions | umls-concept:C1846672 | lld:lifeskim |
pubmed-article:18036232 | lifeskim:mentions | umls-concept:C1425226 | lld:lifeskim |
pubmed-article:18036232 | pubmed:dateCreated | 2008-1-29 | lld:pubmed |
pubmed-article:18036232 | pubmed:abstractText | There is a marked variation in clinical phenotypes that have been associated with mutations in FKRP, ranging from severe congenital muscular dystrophies to limb-girdle muscular dystrophy type 2I (LGMD2I). | lld:pubmed |
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pubmed-article:18036232 | pubmed:language | eng | lld:pubmed |
pubmed-article:18036232 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18036232 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18036232 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18036232 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18036232 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18036232 | pubmed:issn | 1471-2474 | lld:pubmed |
pubmed-article:18036232 | pubmed:author | pubmed-author:DarrasBasil... | lld:pubmed |
pubmed-article:18036232 | pubmed:author | pubmed-author:KunkelLouis... | lld:pubmed |
pubmed-article:18036232 | pubmed:author | pubmed-author:KangPeter BPB | lld:pubmed |
pubmed-article:18036232 | pubmed:author | pubmed-author:AmatoAnthony... | lld:pubmed |
pubmed-article:18036232 | pubmed:author | pubmed-author:EstrellaElici... | lld:pubmed |
pubmed-article:18036232 | pubmed:author | pubmed-author:FeenerChris... | lld:pubmed |
pubmed-article:18036232 | pubmed:author | pubmed-author:ThorneMariell... | lld:pubmed |
pubmed-article:18036232 | pubmed:author | pubmed-author:WhiteAlexande... | lld:pubmed |
pubmed-article:18036232 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18036232 | pubmed:volume | 8 | lld:pubmed |
pubmed-article:18036232 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18036232 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18036232 | pubmed:pagination | 115 | lld:pubmed |
pubmed-article:18036232 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
pubmed-article:18036232 | pubmed:meshHeading | pubmed-meshheading:18036232... | lld:pubmed |
pubmed-article:18036232 | pubmed:meshHeading | pubmed-meshheading:18036232... | lld:pubmed |
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pubmed-article:18036232 | pubmed:meshHeading | pubmed-meshheading:18036232... | lld:pubmed |
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pubmed-article:18036232 | pubmed:meshHeading | pubmed-meshheading:18036232... | lld:pubmed |
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pubmed-article:18036232 | pubmed:meshHeading | pubmed-meshheading:18036232... | lld:pubmed |
pubmed-article:18036232 | pubmed:meshHeading | pubmed-meshheading:18036232... | lld:pubmed |
pubmed-article:18036232 | pubmed:meshHeading | pubmed-meshheading:18036232... | lld:pubmed |
pubmed-article:18036232 | pubmed:meshHeading | pubmed-meshheading:18036232... | lld:pubmed |
pubmed-article:18036232 | pubmed:meshHeading | pubmed-meshheading:18036232... | lld:pubmed |
pubmed-article:18036232 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:18036232 | pubmed:articleTitle | LGMD2I in a North American population. | lld:pubmed |
pubmed-article:18036232 | pubmed:affiliation | Program in Genomics, Children's Hospital Boston and Harvard Medical School, Boston, USA. peter.kang@childrens.harvard.edu | lld:pubmed |
pubmed-article:18036232 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18036232 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:18036232 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |