Claire Donger

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy et al. · Nature Genetics · 1997 · 881 citations

Novel Mutation, Channelopathies, Cardiomyopathy +10

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

Claire Donger, Isabelle Denjoy, Myriam Berthet et al. · Circulation · 1997 · 346 citations

Mutation in the Human Acetylcholinesterase-Associated Collagen Gene, COLQ, Is Responsible for Congenital Myasthenic Syndrome with End-Plate Acetylcholinesterase Deficiency (Type Ic)

Claire Donger, Éric Krejci, Adolf Pou Serradell et al. · The American Journal of Human Genetics · 1998 · 160 citations · Full text

Mendelian Disorder, Connective Tissue Disease, Genetic Disorder +9

Genomic Organization of the <i>KCNQ1</i> K ⁺ Channel Gene and Identification of C-Terminal Mutations in the Long-QT Syndrome

Nathalie Neyroud, Pascale Richard, Nicolas Vignier et al. · Circulation Research · 1999 · 113 citations

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

Myriam Berthet, Isabelle Denjoy, Claire Donger et al. · Circulation · 1999 · 104 citations · Full text