Linked Life Data

18661274

Source:http://linkedlifedata.com/resource/pubmed/id/18661274

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2008-7-28
pubmed:abstractText
To report a novel mutation in the keratin 12 gene (KRT12) found in a Japanese family in association with Meesmann corneal dystrophy (MECD).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0021-5155
pubmed:author
pubmed:issnType
Print
pubmed:volume
52
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
224-6
pubmed:meshHeading
pubmed:articleTitle
A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy.
pubmed:affiliation
Department of Ophthalmology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo, Japan. setomail@med.juntendo.ac.jp
pubmed:publicationType
Journal Article, Case Reports