Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2010-12-17
pubmed:abstractText
Hypertrophic cardiomyopathy (HCM) is one of the most common genetic cardiovascular disorders. Mutations in the MYBPC3 gene are one of the most frequent genetic causes of HCM.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1916-7075
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
26
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
518-22
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Two novel mutations of the MYBPC3 gene identified in Chinese families with hypertrophic cardiomyopathy.
pubmed:affiliation
Department of Cardiology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu Province, China.
pubmed:publicationType
Journal Article, Comparative Study