Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population

Approved

Authors of the publication

Number of authors
18
Authors
Jääskeläinen P, Heliö T, Aalto-Setälä K, Kaartinen M, Ilveskoski E, Hämäläinen L, Melin J, Nieminen MS, Laakso M, Kuusisto J; FinHCM study group, Kervinen H, Mustonen J, Juvonen J, Niemi M, Uusimaa P, Huttunen M, Kotila M, Pietilä M.

Publication channel information

Title of journal/series
Annals of medicine
ISSN (print)
0785-3890
ISSN (electronic)
1365-2060
ISSN (linking)
0785-3890
Publication forum ID
51237
Publication forum level
2
Country of publication
United Kingdom
Internationality
Yes

Detailed publication information

Publication year
2013
Reporting year
2013
Journal/series volume number
45
Page numbers
85-90
DOI
10.3109/07853890.2012.671534

Co-publication information

International co-publication
No

Classification and additional information

MinEdu field of science classification
3121 General medicine, internal medicine and other clinical medicine
Additional information
DOI: 10.3109/07853890.2012.671534,