The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.

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Bibliographic Details
Title: The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.
Authors: Havndrup, O1 (AUTHOR), Bundgaard, H (AUTHOR), Andersen, P S (AUTHOR), Larsen, L A (AUTHOR), Vuust, J (AUTHOR), Kjeldsen, K (AUTHOR), Christiansen, M (AUTHOR)
Source: American Journal of Cardiology. 6/1/2001, Vol. 87 Issue 11, p1315-1317. 3p.
Database: Academic Search Ultimate
Description
ISSN:00029149
DOI:10.1016/s0002-9149(01)01532-6