Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2011-5-9
pubmed:abstractText
Congenital cataract is a clinically and genetically heterogeneous lens disorder. The purpose of this study was to identify the mutation responsible for autosomal dominant congenital coralliform cataracts in two Chinese families and to investigate the relationship between virulence genes and lens morphology.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-10892851, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-11381045, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-12011157, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-12084750, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-12676897, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-15041957, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-15064679, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-15161542, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-15451671, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-16030500, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-17217786, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-18035564, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-18079686, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-18334953, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-19216553, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-19390652, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-19633732, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-8724637, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552497-9927684
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1090-0535
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1085-9
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families.
pubmed:affiliation
Department of Opthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
pubmed:publicationType
Journal Article