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

Publication information

OKM publication type
A1
Category
Artikkelit ja abstraktit
Sub category
Tieteelliset aikakauslehtiartikkelit
Type
Alkuperäisartikkeli
Refereed
Kyllä

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
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,