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- W2900523291 abstract "The myosin heavy chain 7 ( MYH7 ) gene encodes a beta-myosin heavy chain isoform that is expressed primarily in the heart. MYH7 mutations are inherited in an autosomal dominant manner and are believed to cause familial hypertrophic cardiomyopathy (HCM) in about 30% of cases [(1)][1]. Compared with" @default.
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- W2900523291 date "2018-11-01" @default.
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- W2900523291 title "Atrial Arrhythmias and Extensive Left Atrial Fibrosis as the Initial Presentation of MYH7 Gene Mutation" @default.
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- W2900523291 doi "https://doi.org/10.1016/j.jacep.2018.07.016" @default.
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