Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2005-11-14
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0009-9163
pubmed:author
pubmed:issnType
Print
pubmed:volume
68
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
561-3
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:16283890-Abnormalities, Multiple, pubmed-meshheading:16283890-Amino Acid Sequence, pubmed-meshheading:16283890-Aortic Aneurysm, pubmed-meshheading:16283890-Base Sequence, pubmed-meshheading:16283890-Coronary Angiography, pubmed-meshheading:16283890-DNA Mutational Analysis, pubmed-meshheading:16283890-Gene Frequency, pubmed-meshheading:16283890-Genetic Testing, pubmed-meshheading:16283890-Haplotypes, pubmed-meshheading:16283890-Humans, pubmed-meshheading:16283890-Korea, pubmed-meshheading:16283890-Marfan Syndrome, pubmed-meshheading:16283890-Microfilament Proteins, pubmed-meshheading:16283890-Mutation, pubmed-meshheading:16283890-Pedigree, pubmed-meshheading:16283890-Protein-Serine-Threonine Kinases, pubmed-meshheading:16283890-Receptors, Transforming Growth Factor beta, pubmed-meshheading:16283890-Syndrome
pubmed:year
2005
pubmed:articleTitle
Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome.
pubmed:publicationType
Letter, Comment, Case Reports, Research Support, Non-U.S. Gov't