An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Jamie D. Kapplinger, David J. Tester, Mariëlle Alders, +26

Heart Rhythm

ChannelopathiesCardiomyopathyGenetic DisorderGeneticsPhysiology +5

<i>KVLQT1</i> C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome

Claire Donger, Isabelle Denjoy, Myriam Berthet, +7

Circulation

The genetics underlying acquired long QT syndrome: impact for genetic screening

Hideki Itoh, Lia Crotti, Takeshi Aiba, +19

European Heart Journal

<i>MOG1</i>

Darouna Kattygnarath, Svetlana Maugenre, Nathalie Neyroud, +15

Circulation Cardiovascular Genetics

Long QT syndrome in neonates

Jean‐Marc Lupoglazoff, Isabelle Denjoy, E Villain, +7

Journal of the American College of Cardiology

NeonatologyPediatricsNewborn MedicineCongenital Heart DefectMedicine +1

Notched T Waves on Holter Recordings Enhance Detection of Patients With LQT2 ( <i>HERG</i> ) Mutations

Jean‐Marc Lupoglazoff, Isabelle Denjoy, Myriam Berthet, +10

Circulation

Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study

Elijah R. Behr, Eleonora Savio‐Galimberti, Julien Barc, +29

Cardiovascular Research

C-terminal <i>HERG</i> Mutations

Myriam Berthet, Isabelle Denjoy, Claire Donger, +10

Circulation

Homozygous <i>SCN5A</i> Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block

Jean‐Marc Lupoglazoff, T. Cheav, Ghayath Baroudi, +6

Circulation Research

Female Predominance and Transmission Distortion in the Long-QT Syndrome

Medea Imboden, Heikki Swan, Isabelle Denjoy, +12

New England Journal of Medicine