TNNI3 and KCNQ1 co-inherited variants in a family with hypertrophic cardiomyopathy and long QT phenotypes: A case report-Reference-Cited by-同舟云学术

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

Published:2021-06 Issue: Volume:27 Page:100743
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

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

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference21 articles.

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3. Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2;Splawski;Circulation,2000

4. The molecular basis of long QT syndrome and prospects for therapy;Wang;Mol. Med. Today,1998

5. Prolongation of the QTc interval predicts appropriate implantable cardioverter-defibrillator therapies in hypertrophic cardiomyopathy;Gray;JACC Heart Fail.,2013

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1. Co-occurrence of Spondyloepiphyseal Dysplasia and X-Linked Hypophosphatemia in a Three-Generation Chinese Family;Calcified Tissue International;2023-06-06

2. Long QTc in hypertrophic cardiomyopathy: A consequence of structural myocardial damage or a distinct genetic disease?;Frontiers in Cardiovascular Medicine;2023-04-05

3. Correlation between lactate dehydrogenase and QTc interval prolongation in maintenance hemodialysis patients: a cross-sectional study;Annals of Palliative Medicine;2022-11