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A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension https://t.co/Ju0fFvTXEA
A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension https://t.co/Ju0fFvTXEA
New Research: A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension: Background Liddle syndrome is a form of monogenic hypertension caused by mutations in the three homologous… https://t.co/l2r1RMa