17412879

Source:http://linkedlifedata.com/resource/pubmed/id/17412879

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007589, umls-concept:C0026848, umls-concept:C0079471, umls-concept:C0150312, umls-concept:C0206530, umls-concept:C1314792, umls-concept:C1511938, umls-concept:C1879547
pubmed:issue	7
pubmed:dateCreated	2007-7-2
pubmed:abstractText	Rare reports on patients with congenital myopathy with excess of muscle spindles (CMEMS), hypertrophic cardiomyopathy and variable features resembling Noonan syndrome have been published, but the genetic basis of this condition is so far unknown.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-10995764, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-11095964, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-11150980, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-11173924, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-12187941, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-12495620, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-12561057, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-1362901, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-15302938, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-15582775, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-15843272, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-16170316, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-16203995, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-16329078, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-16372351, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-16443854, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-16825433, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-16987887, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-17056636, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-2548731, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-3543368, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-3600660, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-6330729, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-7514502, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-7565669, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-7787238, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-8626650, http://linkedlifedata.com/resource/pubmed/commentcorrection/17412879-8960317
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/HRAS protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins p21(ras)
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1468-6244
pubmed:author	pubmed-author:AhmadianMohammad RezaMR, pubmed-author:BarrosoCândidaC, pubmed-author:DiemAngelikaA, pubmed-author:DvorskyRadovanR, pubmed-author:KratzChristian PCP, pubmed-author:KupskyWilliamW, pubmed-author:NadrooAliA, pubmed-author:StassouStephaniS, pubmed-author:ZenkerMartinM, pubmed-author:van der BurgtInekeI
pubmed:issnType	Electronic
pubmed:volume	44
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	459-62
pubmed:dateRevised	2010-9-15
pubmed:meshHeading	pubmed-meshheading:17412879-Abnormalities, Multiple, pubmed-meshheading:17412879-Amino Acid Sequence, pubmed-meshheading:17412879-Base Sequence, pubmed-meshheading:17412879-Germ-Line Mutation, pubmed-meshheading:17412879-Humans, pubmed-meshheading:17412879-Molecular Sequence Data, pubmed-meshheading:17412879-Muscle Spindles, pubmed-meshheading:17412879-Muscular Diseases, pubmed-meshheading:17412879-Proto-Oncogene Proteins p21(ras), pubmed-meshheading:17412879-Sequence Analysis, DNA, pubmed-meshheading:17412879-Signal Transduction
pubmed:year	2007
pubmed:articleTitle	Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation.
pubmed:publicationType	Letter, Comparative Study, Case Reports, Research Support, Non-U.S. Gov't