17918228

Source:http://linkedlifedata.com/resource/pubmed/id/17918228

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:C0023520, umls-concept:C0026609, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0205082, umls-concept:C0277785, umls-concept:C0332197, umls-concept:C0332281, umls-concept:C0449450, umls-concept:C1418915
pubmed:issue	4
pubmed:dateCreated	2008-5-26
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235742
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Basic Helix-Loop-Helix..., http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/OLIG2 protein, human
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	1552-485X
pubmed:author	pubmed-author:Boespflug-TanguyOdileO, pubmed-author:Bonnet-DupeyronMarie-NoelleMN, pubmed-author:CombesPatriciaP, pubmed-author:Vaurs-BarrièreCatherineC
pubmed:issnType	Electronic
pubmed:day	5
pubmed:volume	147B
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	538-9
pubmed:meshHeading	pubmed-meshheading:17918228-Basic Helix-Loop-Helix Transcription Factors, pubmed-meshheading:17918228-Demyelinating Diseases, pubmed-meshheading:17918228-Humans, pubmed-meshheading:17918228-Motor Neuron Disease, pubmed-meshheading:17918228-Mutation, pubmed-meshheading:17918228-Nerve Tissue Proteins, pubmed-meshheading:17918228-Pelizaeus-Merzbacher Disease
pubmed:year	2008
pubmed:articleTitle	Absence of OLIG2 mutations in patients presenting with a severe Pelizaeus-Merzbacher-like leukodystrophy associated with motor neuron dysfunction.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't