Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2006-9-18
pubmed:abstractText
Dilated cardiomyopathy (DCM) is familial in about 20-35% of patients. The most frequently encountered mutations associated with DCM are found in LMNA.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0022-9032
pubmed:author
pubmed:issnType
Print
pubmed:volume
64
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
812-9; discussion 820-1
pubmed:meshHeading
pubmed-meshheading:16981056-Adolescent, pubmed-meshheading:16981056-Adult, pubmed-meshheading:16981056-Cardiomyopathy, Dilated, pubmed-meshheading:16981056-Child, pubmed-meshheading:16981056-DNA Mutational Analysis, pubmed-meshheading:16981056-Female, pubmed-meshheading:16981056-Genetic Predisposition to Disease, pubmed-meshheading:16981056-Heart Transplantation, pubmed-meshheading:16981056-Humans, pubmed-meshheading:16981056-Lamin Type A, pubmed-meshheading:16981056-Lamins, pubmed-meshheading:16981056-Male, pubmed-meshheading:16981056-Mutation, Missense, pubmed-meshheading:16981056-Myocardium, pubmed-meshheading:16981056-Nuclear Lamina, pubmed-meshheading:16981056-Pedigree, pubmed-meshheading:16981056-Predictive Value of Tests, pubmed-meshheading:16981056-Prevalence, pubmed-meshheading:16981056-Statistics, Nonparametric
pubmed:year
2006
pubmed:articleTitle
Dilated cardiomyopathy caused by LMNA mutations. Clinical and morphological studies.
pubmed:affiliation
Instytut Kardiologii ul. Alpejska 42, 04-628 Warsaw, Poland. zbilinska@ikard.pl
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't