15811014

Source:http://linkedlifedata.com/resource/pubmed/id/15811014

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0026882, umls-concept:C0205396, umls-concept:C0410203, umls-concept:C0410916, umls-concept:C0439064
pubmed:issue	5
pubmed:dateCreated	2005-4-6
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0253664
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatases, http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatases..., http://linkedlifedata.com/resource/pubmed/chemical/myotubularin
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0009-9163
pubmed:author	pubmed-author:DOR, pubmed-author:DolphinCC, pubmed-author:FriendKK, pubmed-author:GattasMM, pubmed-author:HarveyPP, pubmed-author:YuSS
pubmed:issnType	Print
pubmed:volume	67
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	441-2
pubmed:dateRevised	2007-11-15
pubmed:meshHeading	pubmed-meshheading:15811014-Child, pubmed-meshheading:15811014-Child, Preschool, pubmed-meshheading:15811014-Chromosomes, Human, X, pubmed-meshheading:15811014-DNA Mutational Analysis, pubmed-meshheading:15811014-Fatal Outcome, pubmed-meshheading:15811014-Genotype, pubmed-meshheading:15811014-Humans, pubmed-meshheading:15811014-Infant, Newborn, pubmed-meshheading:15811014-Male, pubmed-meshheading:15811014-Mutation, Missense, pubmed-meshheading:15811014-Myopathies, Structural, Congenital, pubmed-meshheading:15811014-Pedigree, pubmed-meshheading:15811014-Phenotype, pubmed-meshheading:15811014-Protein Tyrosine Phosphatases, pubmed-meshheading:15811014-Protein Tyrosine Phosphatases, Non-Receptor
pubmed:year	2005
pubmed:articleTitle	X-linked myotubular myopathy: mutation R69C identified in a family with multiple neonatal deaths.
pubmed:publicationType	Letter, Case Reports