4544952

Source:http://linkedlifedata.com/resource/pubmed/id/4544952

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011155, umls-concept:C0221061, umls-concept:C0332307, umls-concept:C0439661, umls-concept:C1314792
pubmed:dateCreated	1974-6-5
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/1270475
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0077-0078
pubmed:author	pubmed-author:FrühDD, pubmed-author:JaegerWW, pubmed-author:LauerH JHJ
pubmed:issnType	Print
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	145-7
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:4544952-Color Vision Defects, pubmed-meshheading:4544952-Genes, Dominant, pubmed-meshheading:4544952-Germany, West, pubmed-meshheading:4544952-Humans, pubmed-meshheading:4544952-Optic Atrophy
pubmed:year	1972
pubmed:articleTitle	Types of acquired colour deficiencies caused by autosomal-dominant infantile optic atrophy.
pubmed:publicationType	Journal Article