18592125

Source:http://linkedlifedata.com/resource/pubmed/id/18592125

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0162735, umls-concept:C0205314, umls-concept:C0205713, umls-concept:C0679622, umls-concept:C1418677
pubmed:issue	9
pubmed:dateCreated	2008-10-29
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0423161
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Myelin Proteins, http://linkedlifedata.com/resource/pubmed/chemical/PMP22 protein, human
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0340-5354
pubmed:author	pubmed-author:BesonBB, pubmed-author:HollandN RNR, pubmed-author:ParkeJ TJT, pubmed-author:ProdanC ICI, pubmed-author:ZubairSS
pubmed:issnType	Print
pubmed:volume	255
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1417-8
pubmed:dateRevised	2009-4-2
pubmed:meshHeading	pubmed-meshheading:18592125-Charcot-Marie-Tooth Disease, pubmed-meshheading:18592125-Child, Preschool, pubmed-meshheading:18592125-Family Health, pubmed-meshheading:18592125-Female, pubmed-meshheading:18592125-Humans, pubmed-meshheading:18592125-Male, pubmed-meshheading:18592125-Middle Aged, pubmed-meshheading:18592125-Myelin Proteins, pubmed-meshheading:18592125-Pedigree, pubmed-meshheading:18592125-Point Mutation, pubmed-meshheading:18592125-Young Adult
pubmed:year	2008
pubmed:articleTitle	A novel point mutation in the PMP22 gene in a family with Roussy-Levy syndrome.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't