8781450

Source:http://linkedlifedata.com/resource/pubmed/id/8781450

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013879, umls-concept:C0015879, umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0205314, umls-concept:C0302583, umls-concept:C0679622, umls-concept:C1524003, umls-concept:C1833213
pubmed:issue	5
pubmed:dateCreated	1996-10-16
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/8781450-7492760
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7603509
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Ferritins, http://linkedlifedata.com/resource/pubmed/chemical/Iron
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0006-4971
pubmed:author	pubmed-author:Aguilar-MartinezPP, pubmed-author:BironCC, pubmed-author:JeanjeanPP, pubmed-author:MasmejeanCC, pubmed-author:SchvedJ FJF
pubmed:issnType	Print
pubmed:day	1
pubmed:volume	88
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1895
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:8781450-Adult, pubmed-meshheading:8781450-Cataract, pubmed-meshheading:8781450-Child, pubmed-meshheading:8781450-DNA Mutational Analysis, pubmed-meshheading:8781450-Female, pubmed-meshheading:8781450-Ferritins, pubmed-meshheading:8781450-Gene Expression Regulation, pubmed-meshheading:8781450-Genes, pubmed-meshheading:8781450-Humans, pubmed-meshheading:8781450-Iron, pubmed-meshheading:8781450-Male, pubmed-meshheading:8781450-Point Mutation, pubmed-meshheading:8781450-Syndrome
pubmed:year	1996
pubmed:articleTitle	A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome.
pubmed:publicationType	Letter, Comment, Case Reports