9143933

Source:http://linkedlifedata.com/resource/pubmed/id/9143933

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015295, umls-concept:C0017337, umls-concept:C0030705, umls-concept:C0205711, umls-concept:C0533932, umls-concept:C0599155
pubmed:issue	5
pubmed:dateCreated	1997-7-17
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9215429
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Myelin Proteolipid Protein
pubmed:status	MEDLINE
pubmed:issn	1059-7794
pubmed:author	pubmed-author:InoueKK, pubmed-author:KawanishiCC, pubmed-author:KimuraSS, pubmed-author:KosakaKK, pubmed-author:MiyakawaTT, pubmed-author:OnishiHH, pubmed-author:OsakaHH, pubmed-author:OwaKK, pubmed-author:SuzukiKK, pubmed-author:YamadaYY
pubmed:issnType	Print
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	475-6
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:9143933-Child, Preschool, pubmed-meshheading:9143933-Diffuse Cerebral Sclerosis of Schilder, pubmed-meshheading:9143933-Electroencephalography, pubmed-meshheading:9143933-Exons, pubmed-meshheading:9143933-Humans, pubmed-meshheading:9143933-Magnetic Resonance Imaging, pubmed-meshheading:9143933-Male, pubmed-meshheading:9143933-Myelin Proteolipid Protein, pubmed-meshheading:9143933-Point Mutation, pubmed-meshheading:9143933-Polymerase Chain Reaction
pubmed:year	1997
pubmed:articleTitle	A new missense mutation in exon 6 of the proteolipid protein gene in a patient with Pelizaeus-Merzbacher disease.
pubmed:affiliation	Department of Psychiatry, Yokohama City University, Japan.
pubmed:publicationType	Journal Article, Case Reports