Linked Life Data

16424523

Source:http://linkedlifedata.com/resource/pubmed/id/16424523

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2006-1-20
pubmed:abstractText
To determine if asymptomatic carriers from a previously identified large pedigree of the Leber's hereditary optic neuropathy (LHON) 11778 mtDNA mutation have colour vision deficits.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-10072046, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-10347173, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-10360310, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-10976107, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-11181859, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-11190025, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-12545691, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-13996879, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-1417830, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-1674640, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-1928099, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-2579042, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-3201231, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-6976039, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-6979252, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-7314519, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-8240102, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-8489411, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-8719696, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-9191778, http://linkedlifedata.com/resource/pubmed/commentcorrection/16424523-9345284
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0007-1161
pubmed:author
pubmed:issnType
Print
pubmed:volume
90
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
150-3
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2006
pubmed:articleTitle
Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study.
pubmed:affiliation
Doheny Eye Institute, 1450 San Pablo Street, Los Angeles, CA 90033, USA. pquiros@usc.edu
pubmed:publicationType
Journal Article