| pubmed-article:10599760 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10599760 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
| pubmed-article:10599760 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:10599760 | lifeskim:mentions | umls-concept:C0037492 | lld:lifeskim |
| pubmed-article:10599760 | lifeskim:mentions | umls-concept:C0238358 | lld:lifeskim |
| pubmed-article:10599760 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:10599760 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:10599760 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:10599760 | pubmed:dateCreated | 2000-1-4 | lld:pubmed |
| pubmed-article:10599760 | pubmed:abstractText | To identify the cause of hypokalemic periodic paralysis (HOKPP) in a family whose disease is not caused by a mutation in the dihydropyridine-sensitive (DHP) receptor alpha1-subunit gene (CACNA1S). | lld:pubmed |
| pubmed-article:10599760 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10599760 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10599760 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:10599760 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10599760 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:10599760 | pubmed:issn | 0028-3878 | lld:pubmed |
| pubmed-article:10599760 | pubmed:author | pubmed-author:EbersG CGC | lld:pubmed |
| pubmed-article:10599760 | pubmed:author | pubmed-author:BulmanD EDE | lld:pubmed |
| pubmed-article:10599760 | pubmed:author | pubmed-author:HaleC GCG | lld:pubmed |
| pubmed-article:10599760 | pubmed:author | pubmed-author:NicolleM WMW | lld:pubmed |
| pubmed-article:10599760 | pubmed:author | pubmed-author:ScogganK AKA | lld:pubmed |
| pubmed-article:10599760 | pubmed:author | pubmed-author:van OeneM DMD | lld:pubmed |
| pubmed-article:10599760 | pubmed:author | pubmed-author:TollarL LLL | lld:pubmed |
| pubmed-article:10599760 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10599760 | pubmed:day | 10 | lld:pubmed |
| pubmed-article:10599760 | pubmed:volume | 53 | lld:pubmed |
| pubmed-article:10599760 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10599760 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10599760 | pubmed:pagination | 1932-6 | lld:pubmed |
| pubmed-article:10599760 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:10599760 | pubmed:meshHeading | pubmed-meshheading:10599760... | lld:pubmed |
| pubmed-article:10599760 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10599760 | pubmed:articleTitle | A novel sodium channel mutation in a family with hypokalemic periodic paralysis. | lld:pubmed |
| pubmed-article:10599760 | pubmed:affiliation | Division of Neurology, Ottawa General Hospital, Ottawa Hospital Research Institute, Ontario, Canada. dbulman@ogh.on.ca | lld:pubmed |
| pubmed-article:10599760 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10599760 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:10599760 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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