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Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication. https://t.co/BNEmM43M7A #longqt #cardiotwitter #epeeps
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication. https://t.co/BNEmM43M7A #longqt #cardiotwitter #epeeps
New Research: Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication: Background: Pathogenic mutations in the KCNH2 gene were associated with long QT… https://t.co/T9a