|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0001792,
umls-concept:C0007194,
umls-concept:C0012359,
umls-concept:C0017337,
umls-concept:C0030705,
umls-concept:C0205314,
umls-concept:C0242698,
umls-concept:C0599155,
umls-concept:C0679622,
umls-concept:C1149266,
umls-concept:C1273518
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|
pubmed:issue |
5
|
|
pubmed:dateCreated |
2003-3-11
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|
pubmed:abstractText |
We studied the clinical features of hypertrophic cardiomyopathy (HCM) caused by a novel mutation in the myosin binding protein-C (MyBP-C) gene in patients and family members of Japanese descent.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
0735-1097
|
|
pubmed:author |
pubmed-author:HayashiKenshiK,
pubmed-author:HayashiTatsumiT,
pubmed-author:InoHidekazuH,
pubmed-author:InoueMasaruM,
pubmed-author:KanedaTomoyaT,
pubmed-author:KiyamaMasaruM,
pubmed-author:KonnoTetsuoT,
pubmed-author:MabuchiHiroshiH,
pubmed-author:MabuchiTomohitoT,
pubmed-author:MatsuyamaToruT,
pubmed-author:SakataKenjiK,
pubmed-author:ShimizuMasamiM,
pubmed-author:TeraiHidenobuH,
pubmed-author:YamaguchiMasatoM
|
|
pubmed:issnType |
Print
|
|
pubmed:day |
5
|
|
pubmed:volume |
41
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
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pubmed:pagination |
781-6
|
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:12628722-Adolescent,
pubmed-meshheading:12628722-Adult,
pubmed-meshheading:12628722-Age Distribution,
pubmed-meshheading:12628722-Aged,
pubmed-meshheading:12628722-Cardiomyopathy, Dilated,
pubmed-meshheading:12628722-Cardiomyopathy, Hypertrophic,
pubmed-meshheading:12628722-Carrier Proteins,
pubmed-meshheading:12628722-Cohort Studies,
pubmed-meshheading:12628722-Comorbidity,
pubmed-meshheading:12628722-Echocardiography,
pubmed-meshheading:12628722-Electrocardiography,
pubmed-meshheading:12628722-Female,
pubmed-meshheading:12628722-Genetic Predisposition to Disease,
pubmed-meshheading:12628722-Genetic Testing,
pubmed-meshheading:12628722-Humans,
pubmed-meshheading:12628722-Japan,
pubmed-meshheading:12628722-Male,
pubmed-meshheading:12628722-Middle Aged,
pubmed-meshheading:12628722-Mutation, Missense,
pubmed-meshheading:12628722-Pedigree,
pubmed-meshheading:12628722-Polymerase Chain Reaction,
pubmed-meshheading:12628722-Polymorphism, Genetic,
pubmed-meshheading:12628722-Prevalence,
pubmed-meshheading:12628722-Risk Assessment,
pubmed-meshheading:12628722-Severity of Illness Index,
pubmed-meshheading:12628722-Survival Rate,
pubmed-meshheading:12628722-Ventricular Dysfunction, Left
|
|
pubmed:year |
2003
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|
pubmed:articleTitle |
A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients.
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|
pubmed:affiliation |
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
|
|
pubmed:publicationType |
Journal Article,
Comparative Study
|
