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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

✍ Scribed by Ole Havndrup; Henning Bundgaard; Paal S. Andersen; Lars A. Larsen; Jens Vuust; Keld Kjeldsen; Michael Christiansen


Book ID
113974777
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
113 KB
Volume
87
Category
Article
ISSN
0002-9149

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