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Authors
Benkirane, Mehdi https://orcid.org/0000-0001-6445-6347
Marelli, Cecilia
Guissart, Claire
Roubertie, Agathe
Ollagnon, Elizabeth
Choumert, Ariane
Fluchère, Frédérique
Magne, Fabienne Ory
Halleb, Yosra
Renaud, Mathilde
Larrieu, Lise
Baux, David
Patat, Olivier
Bousquet, Idriss
Ravel, Jean-Marie
Cuntz-Shadfar, Danielle
Sarret, Catherine
Ayrignac, Xavier
Rolland, Anne
Morales, Raoul
Pointaux, Morgane
Lieutard-Haag, Cathy
Laurens, Brice
Tillikete, Caroline
Bernard, Emilien
Mallaret, Martial
Carra-Dallière, Clarisse
Tranchant, Christine
Meyer, Pierre
Damaj, Lena
Pasquier, Laurent
Acquaviva, Cecile
Chaussenot, Annabelle
Isidor, Bertrand
Nguyen, Karine
Camu, William
Eusebio, Alexandre
Carrière, Nicolas
Riquet, Audrey
Thouvenot, Eric
Gonzales, Victoria
Carme, Emilie
Attarian, Shahram
Odent, Sylvie
Castrioto, Anna
Ewenczyk, Claire
Charles, Perrine
Kremer, Laurent
Sissaoui, Samira
Bahi-buisson, Nadia
Kaphan, Elsa
Degardin, Adrian
Doray, Bérénice
Julia, Sophie
Remerand, Ganaëlle
Fraix, Valerie
Haidar, Lydia Abou
Lazaro, Leila
Laugel, Vincent
Villega, Frederic
Charlin, Cyril
Frismand, Solène
Moreira, Marinha Costa
Witjas, Tatiana
Francannet, Christine
Walther-Louvier, Ulrike
Fradin, Mélanie
Chabrol, Brigitte
Fluss, Joel
Bieth, Eric
Castelnovo, Giovanni
Vergnet, Sylvain
Meunier, Isabelle
Verloes, Alain
Brischoux-Boucher, Elise
Coubes, Christine
Geneviève, David
Lebouc, Nicolas
Azulay, Jean Phillipe
Anheim, Mathieu
Goizet, Cyril
Rivier, François
Labauge, Pierre
Calvas, Patrick
Koenig, Michel
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This article is maintained by: Elsevier
Article Title: High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01250-6
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
