Whole-exome Sequencing Reveals MYH7 P.r671c Mutation in Three Different Phenotypes of Familial Hypertrophic Cardiomyopathy.
Experimental and Therapeutic Medicine（2021）
Key words
familial hypertrophic cardiomyopathy,gene mutation,whole-exome sequencing,myosin heavy chain 7,genotype-phenotype correlation
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