5748751

Source:http://linkedlifedata.com/resource/pubmed/id/5748751

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004134, umls-concept:C0011849, umls-concept:C0015576, umls-concept:C0026846, umls-concept:C0035334, umls-concept:C0205210, umls-concept:C0439660, umls-concept:C0684224
pubmed:issue	10
pubmed:dateCreated	1969-1-8
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0028-3878
pubmed:author	pubmed-author:FurukawaTT, pubmed-author:NakaiMM, pubmed-author:SugitaHH, pubmed-author:TakagiAA, pubmed-author:TsukagoshiHH
pubmed:issnType	Print
pubmed:volume	18
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	942-7
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:5748751-Adolescent, pubmed-meshheading:5748751-Adult, pubmed-meshheading:5748751-Cerebellar Ataxia, pubmed-meshheading:5748751-Diabetes Complications, pubmed-meshheading:5748751-Electroencephalography, pubmed-meshheading:5748751-Electromyography, pubmed-meshheading:5748751-Evoked Potentials, pubmed-meshheading:5748751-Female, pubmed-meshheading:5748751-Genes, Dominant, pubmed-meshheading:5748751-Humans, pubmed-meshheading:5748751-Male, pubmed-meshheading:5748751-Middle Aged, pubmed-meshheading:5748751-Muscular Atrophy, pubmed-meshheading:5748751-Pedigree, pubmed-meshheading:5748751-Retinitis Pigmentosa, pubmed-meshheading:5748751-Sex Factors, pubmed-meshheading:5748751-Time Factors
pubmed:year	1968
pubmed:articleTitle	Hereditary muscular atrophy with ataxia, retinitis pigmentosa, and diabetes mellitus. A clinical report of a family.
pubmed:publicationType	Journal Article