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Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

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


Book ID
110025596
Publisher
Nature Publishing Group
Year
2004
Tongue
English
Weight
124 KB
Volume
12
Category
Article
ISSN
1018-4813

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