12471219

Source:http://linkedlifedata.com/resource/pubmed/id/12471219

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0270922, umls-concept:C0332281, umls-concept:C0376249, umls-concept:C1414315
pubmed:issue	12
pubmed:dateCreated	2002-12-9
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/EGR2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Early Growth Response Protein 2, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1468-6244
pubmed:author	pubmed-author:BoucheratMM, pubmed-author:BoutrandLL, pubmed-author:ChazotGG, pubmed-author:GatignolAA, pubmed-author:LatourPP, pubmed-author:UpadhyayaMM, pubmed-author:VandenbergheAA, pubmed-author:VandenbergheNN
pubmed:issnType	Electronic
pubmed:volume	39
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	e81
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:12471219-Charcot-Marie-Tooth Disease, pubmed-meshheading:12471219-DNA Mutational Analysis, pubmed-meshheading:12471219-DNA-Binding Proteins, pubmed-meshheading:12471219-Early Growth Response Protein 2, pubmed-meshheading:12471219-Female, pubmed-meshheading:12471219-Gene Frequency, pubmed-meshheading:12471219-Genetic Testing, pubmed-meshheading:12471219-Hereditary Central Nervous System Demyelinating Diseases, pubmed-meshheading:12471219-Humans, pubmed-meshheading:12471219-Male, pubmed-meshheading:12471219-Mutation, pubmed-meshheading:12471219-Phenotype, pubmed-meshheading:12471219-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:12471219-Transcription Factors, pubmed-meshheading:12471219-Zinc Fingers
pubmed:year	2002
pubmed:articleTitle	Frequency of mutations in the early growth response 2 gene associated with peripheral demyelinating neuropathies.
pubmed:affiliation	Laboratoire de Génétique Moléculaire Humaine, Université Claude Bernard, Lyon 1, France. vandenbe@rockefeller.univ-lyon1.fr
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't