Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes

scientific article

Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

External links are
P356DOI10.1080/07853890310017161
P3181OpenCitations bibliographic resource ID1037689
P698PubMed publication ID15000344

P50authorMarkku LaaksoQ28050161
Johanna KuusistoQ28516669
Lauri ToivonenQ112404693
Pertti JääskeläinenQ117282169
Raija MiettinenQ117282170
P2093author name stringPäivi Kärkkäinen
P2860cites workSarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderlyQ24292234
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomereQ24316399
Disease gene mapping in isolated human populations: the example of FinlandQ24514989
First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathyQ28198455
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathyQ28268916
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathyQ28284626
Hypertrophic cardiomyopathy in Tuscany: clinical course and outcome in an unselected regional population.Q33173620
Molecular genetics of the Finnish disease heritage.Q33724113
Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease geneQ33872178
The molecular genetic basis for hypertrophic cardiomyopathyQ33939892
Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathyQ34120159
Molecular genetic studies of familial hypertrophic cardiomyopathyQ40829741
The management of hypertrophic cardiomyopathyQ41366322
Clinical course of hypertrophic cardiomyopathy in a regional United States cohortQ43565120
Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin GeneQ57279251
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectFinlandQ33
hypertrophic cardiomyopathyQ1364270
P304page(s)23-32
P577publication date2004-01-01
P1433published inAnnals of MedicineQ4767853
P1476titleGenetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes
P478volume36