High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families

Mehdi Benkirane, Cécilia Marelli, Claire Guissart, Agathe Roubertie, Elizabeth Ollagnon, Ariane Choumert, Frédérique Fluchère, Fabienne Ory Magne, Yosra Halleb, M. Renaud, Lise Larrieu, David Baux, Olivier Patat, Idriss Bousquet, Jean‐Marie Ravel, Danielle Cuntz-Shadfar, Catherine Sarret, Xavier Ayrignac, Anne Rolland, Raúl Juntas‐Morales, Morgane Pointaux, Cathy Lieutard-Haag, Brice Laurens, Caroline Tillikete, E Bernard, Martial Mallaret, Clarisse Carra‐Dallière, Christine Tranchant, Pierre Meyer, Léna Damaj, Laurent Pasquier, Cécile Acquaviva, Annabelle Chaussenot, Bertrand Isidor, Karine Nguyen, William Camu, Alexandre Eusébio, Nicolas Carrière, Audrey Riquet, Éric Thouvenot, Victoria Gonzales, Emilie Carme, Shahram Attarian, Sylvie Odent, Anna Castrioto, Claire Ewenczyk, Perrine Charles, Laurent Kremer, Samira Sissaoui, Nadia Bahi‐Buisson, Elsa Kaphan, Adrian Degardin, Bérénice Doray, Sophie Julia, Ganaëlle Remérand, Valérie Fraix, Lydia Abou Haidar, Leïla Lazaro, Vincent Laugel, Frédéric Villega, Cyril Charlin, Solène Frismand, Marinha Costa Moreira, Tatiana Witjas, Christine Francannet, Ulrike Walther‐Louvier, Mélanie Fradin, B. Chabrol, Joël Fluss, Éric Bieth, Giovanni Castelnovo, Sylvain Vergnet, Isabelle Meunier, Alain Verloès, Elise Brischoux‐Boucher, Christine Coubes, David Geneviève, Nicolas Lebouc, Jean Phillipe Azulay, Mathieu Anheim, Cyril Goizet, François Rivier, Pierre Labauge, Patrick Calvas, Michel Kœnig