Associated Papers
Whole-exome sequencing reveals MYH7 p.R671C mutation in three different phenotypes of familial hypertrophic cardiomyopathy.
Yu W et al.
Experimental and Therapeutic Medicine, 2021
Mutational landscape and potential therapeutic targets for sporadic pancreatic neuroendocrine tumors based on target next-generation sequencing.
Zheng K et al.
Experimental and Therapeutic Medicine, 2021
33747156 (PubMed )
Supplement: Supplementary_Data3.xlsx › Table_SII
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