18846638

Source:http://linkedlifedata.com/resource/pubmed/id/18846638

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012634, umls-concept:C0027888, umls-concept:C0332307, umls-concept:C1415076, umls-concept:C1706510
pubmed:issue	3
pubmed:dateCreated	2008-10-9
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7613873
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Codon, http://linkedlifedata.com/resource/pubmed/chemical/Connexins, http://linkedlifedata.com/resource/pubmed/chemical/connexin 32
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1432-1203
pubmed:author	pubmed-author:BonetHilda BibasHB, pubmed-author:Carrero-ValenzuelaRoque DanielRD, pubmed-author:EpplenJörg ThomasJT, pubmed-author:KöttingJudithJ
pubmed:issnType	Electronic
pubmed:volume	124
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	305-6
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:18846638-Amino Acid Substitution, pubmed-meshheading:18846638-Codon, pubmed-meshheading:18846638-Connexins, pubmed-meshheading:18846638-Hereditary Sensory and Motor Neuropathy, pubmed-meshheading:18846638-Humans, pubmed-meshheading:18846638-Mutation, Missense, pubmed-meshheading:18846638-Point Mutation
pubmed:year	2008
pubmed:articleTitle	Gene symbol: GJB1. Disease: Hereditary motor and sensory neuropathy type X?
pubmed:affiliation	RUHR-Universität Bochum, Humangenetik, Universitätsstrasse, 150, 44801 Bochum, Germany. Judith.Koetting@rub.de
pubmed:publicationType	Journal Article