19380703

Source:http://linkedlifedata.com/resource/pubmed/id/19380703

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030705, umls-concept:C0031437, umls-concept:C0205210, umls-concept:C0337810, umls-concept:C0376249, umls-concept:C0596611
pubmed:issue	16
pubmed:dateCreated	2009-4-21
pubmed:abstractText	The frequency of various limb-girdle muscular dystrophy (LGMD) molecular diagnoses has previously been investigated only in cohorts of patients presenting LGMD phenotype.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CAPN3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Calpain, http://linkedlifedata.com/resource/pubmed/chemical/Caveolin 3, http://linkedlifedata.com/resource/pubmed/chemical/Creatine Kinase, http://linkedlifedata.com/resource/pubmed/chemical/DYSF protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Muscle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Sarcoglycans, http://linkedlifedata.com/resource/pubmed/chemical/emerin
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1526-632X
pubmed:author	pubmed-author:AngeliniCC, pubmed-author:AurinoSS, pubmed-author:FaninMM, pubmed-author:NascimbeniA CAC, pubmed-author:NigroVV, pubmed-author:PegoraroEE, pubmed-author:TascaEE
pubmed:issnType	Electronic
pubmed:day	21
pubmed:volume	72
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1432-5
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:19380703-Adult, pubmed-meshheading:19380703-Age of Onset, pubmed-meshheading:19380703-Calpain, pubmed-meshheading:19380703-Caveolin 3, pubmed-meshheading:19380703-Child, pubmed-meshheading:19380703-Cohort Studies, pubmed-meshheading:19380703-Creatine Kinase, pubmed-meshheading:19380703-DNA Mutational Analysis, pubmed-meshheading:19380703-Female, pubmed-meshheading:19380703-Gene Frequency, pubmed-meshheading:19380703-Genetic Predisposition to Disease, pubmed-meshheading:19380703-Genetic Testing, pubmed-meshheading:19380703-Genotype, pubmed-meshheading:19380703-Humans, pubmed-meshheading:19380703-Italy, pubmed-meshheading:19380703-Male, pubmed-meshheading:19380703-Membrane Proteins, pubmed-meshheading:19380703-Muscle Proteins, pubmed-meshheading:19380703-Muscular Dystrophies, Limb-Girdle, pubmed-meshheading:19380703-Mutation, pubmed-meshheading:19380703-Nuclear Proteins, pubmed-meshheading:19380703-Phenotype, pubmed-meshheading:19380703-Sarcoglycans
pubmed:year	2009
pubmed:articleTitle	Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes.
pubmed:affiliation	Department of Neurosciences, University of Padova, via Giuseppe Orus 2, 35129 Padova, Italy. marina.fanin@unipd.it
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't