19770477

Source:http://linkedlifedata.com/resource/pubmed/id/19770477

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0221055, umls-concept:C0678226, umls-concept:C1416543, umls-concept:C1419862, umls-concept:C1720189
pubmed:issue	12
pubmed:dateCreated	2009-9-22
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/, http://linkedlifedata.com/resource/pubmed/grant/5U54 RR019498-05, http://linkedlifedata.com/resource/pubmed/grant/G0601943
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/KCNA1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Kv1.1 Potassium Channel, http://linkedlifedata.com/resource/pubmed/chemical/SCN4A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Sodium Channels
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	1526-632X
pubmed:author	pubmed-author:HannaM GMG, pubmed-author:KullmannD MDM, pubmed-author:LabrumRR, pubmed-author:MatthewsEE, pubmed-author:RajakulendranSS, pubmed-author:SchorgeSS, pubmed-author:SueSS, pubmed-author:TanS VSV, pubmed-author:TomlinsonS ESE
pubmed:issnType	Electronic
pubmed:day	22
pubmed:volume	73
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	993-5
pubmed:dateRevised	2010-9-24
pubmed:meshHeading	pubmed-meshheading:19770477-Action Potentials, pubmed-meshheading:19770477-Adult, pubmed-meshheading:19770477-Ataxia, pubmed-meshheading:19770477-DNA Mutational Analysis, pubmed-meshheading:19770477-Electromyography, pubmed-meshheading:19770477-Female, pubmed-meshheading:19770477-Genetic Predisposition to Disease, pubmed-meshheading:19770477-Genotype, pubmed-meshheading:19770477-Humans, pubmed-meshheading:19770477-Kv1.1 Potassium Channel, pubmed-meshheading:19770477-Muscle, Skeletal, pubmed-meshheading:19770477-Muscle Contraction, pubmed-meshheading:19770477-Muscle Cramp, pubmed-meshheading:19770477-Muscle Weakness, pubmed-meshheading:19770477-Mutation, pubmed-meshheading:19770477-Myokymia, pubmed-meshheading:19770477-Myotonic Disorders, pubmed-meshheading:19770477-Sodium Channels
pubmed:year	2009
pubmed:articleTitle	A patient with episodic ataxia and paramyotonia congenita due to mutations in KCNA1 and SCN4A.
pubmed:affiliation	Medical Research Council Centre for Neuromuscular Disease, Queen Square, London, WC1N 3BG, UK.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural