Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2007-11-16
pubmed:abstractText
To identify the gene mutation in autosomal dominant Thiel-Behnke corneal dystrophy affecting a five-generation Chinese family. To study the TGFBI gene mutation in Chinese patients with Thiel-Behnke corneal dystrophy by molecular genetic analysis.
pubmed:language
chi
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0412-4081
pubmed:author
pubmed:issnType
Print
pubmed:volume
43
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
718-21
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
[TGFBI gene mutation analysis in a Chinese family with Thiel-Behnke corneal dystrophy].
pubmed:affiliation
Department of Ophthalmology, the Second Affiliated Hospital, Harbin Medical University, Harbin 150086, China. qyh64@hotmail.com
pubmed:publicationType
Journal Article, English Abstract