17548557

Source:http://linkedlifedata.com/resource/pubmed/id/17548557

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0332281, umls-concept:C0599155, umls-concept:C0878544, umls-concept:C1417542, umls-concept:C1844915
pubmed:issue	23
pubmed:dateCreated	2007-6-5
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Cardiac Myosins, http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers, http://linkedlifedata.com/resource/pubmed/chemical/MYH7 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Myosin Heavy Chains, http://linkedlifedata.com/resource/pubmed/chemical/Protein Isoforms, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Ventricular Myosins
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	1526-632X
pubmed:author	pubmed-author:DarinNN, pubmed-author:GilljamTT, pubmed-author:OldforsAA, pubmed-author:Ostman-SmithII, pubmed-author:TajsharghiHH
pubmed:issnType	Electronic
pubmed:day	5
pubmed:volume	68
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2041-2
pubmed:meshHeading	pubmed-meshheading:17548557-Cardiac Myosins, pubmed-meshheading:17548557-Cardiomyopathies, pubmed-meshheading:17548557-Child, pubmed-meshheading:17548557-DNA Mutational Analysis, pubmed-meshheading:17548557-Genetic Markers, pubmed-meshheading:17548557-Genetic Predisposition to Disease, pubmed-meshheading:17548557-Heart, pubmed-meshheading:17548557-Humans, pubmed-meshheading:17548557-Male, pubmed-meshheading:17548557-Muscle, Skeletal, pubmed-meshheading:17548557-Muscle Weakness, pubmed-meshheading:17548557-Muscular Diseases, pubmed-meshheading:17548557-Mutation, Missense, pubmed-meshheading:17548557-Myocardium, pubmed-meshheading:17548557-Myosin Heavy Chains, pubmed-meshheading:17548557-Protein Isoforms, pubmed-meshheading:17548557-RNA, Messenger, pubmed-meshheading:17548557-Ventricular Myosins
pubmed:year	2007
pubmed:articleTitle	New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7.
pubmed:affiliation	Department of Pediatrics, Sahlgrenska University Hospital, Göteborg, Sweden. niklas.darin@vgregion.se
pubmed:publicationType	Journal Article, Case Reports