2614456

Source:http://linkedlifedata.com/resource/pubmed/id/2614456

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007758, umls-concept:C0011053, umls-concept:C0026846, umls-concept:C0027066, umls-concept:C0443147
pubmed:issue	12
pubmed:dateCreated	1990-3-7
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/2614456-2494436, http://linkedlifedata.com/resource/pubmed/commentcorrection/2614456-2646519, http://linkedlifedata.com/resource/pubmed/commentcorrection/2614456-3779373, http://linkedlifedata.com/resource/pubmed/commentcorrection/2614456-5698045
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985191R
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0022-3050
pubmed:author	pubmed-author:FerroJ MJM, pubmed-author:MeloT PTP
pubmed:issnType	Print
pubmed:volume	52
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1448-9
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:2614456-Cerebellar Ataxia, pubmed-meshheading:2614456-Deafness, pubmed-meshheading:2614456-Genes, Dominant, pubmed-meshheading:2614456-Humans, pubmed-meshheading:2614456-Male, pubmed-meshheading:2614456-Middle Aged, pubmed-meshheading:2614456-Muscular Atrophy, pubmed-meshheading:2614456-Myoclonus, pubmed-meshheading:2614456-Syndrome
pubmed:year	1989
pubmed:articleTitle	Autosomal dominant cerebellar ataxia with deafness, myoclonus and amyotrophy.
pubmed:publicationType	Letter, Case Reports