Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2008-2-5
pubmed:abstractText
To study the mutation of FRMD7 gene in a Chinese family with congenital idiopathic nystagmus.
pubmed:language
chi
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1003-9406
pubmed:author
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
11-4
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
[The G990T mutation of the FRMD7 gene in a Chinese family with congenital idiopathic nystagmus].
pubmed:affiliation
Department of Ophthalmic Molecular Genetics, Tianjin Eye Hospital, Tianjin, People's Republic of China.
pubmed:publicationType
Journal Article, English Abstract