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TNNI3 and KCNQ1 co-inherited variants in a family with hypertrophic cardiomyopathy and long QT phenotypes: A case report

QTc prolongation is reported in patients with hypertrophic cardiomyopathy (HCM). However, the causes of the QTc interval increase remain unclear. The main contribution to QTc prolongation in HCM is attributed to the myocardial hypertrophy and related structural damage. In a 24-year-old male proband,...

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Bibliographische Detailangaben
Veröffentlicht in:Mol Genet Metab Rep
Hauptverfasser: Cava, Francesco, Cristiano, Ernesto, Musumeci, Maria Beatrice, Savio, Camilla, Germani, Aldo, Monaco, Maria Lo, Petrucci, Simona, Torrisi, Maria Rosaria, Autore, Camillo, Rubattu, Speranza, Piane, Maria
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2021
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7985525/
https://ncbi.nlm.nih.gov/pubmed/33777698
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgmr.2021.100743
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