Crossmark

Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies

Crossref DOI link: https://doi.org/10.1038/s41436-018-0089-2

Published Print: 2019-03

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Valence, Stéphanie

Cochet, Emmanuelle

Rougeot, Christelle

Garel, Catherine

Chantot-Bastaraud, Sandra

Lainey, Elodie

Afenjar, Alexandra

Barthez, Marie-Anne

Bednarek, Nathalie

Doummar, Diane

Faivre, Laurence

Goizet, Cyril

Haye, Damien

Heron, Bénédicte

Kemlin, Isabelle

Lacombe, Didier

Milh, Mathieu

Moutard, Marie-Laure

Riant, Florence

Robin, Stéphanie

Roubertie, Agathe

Sarda, Pierre

Toutain, Annick

Villard, Laurent

Ville, Dorothée

Billette de Villemeur, Thierry

Rodriguez, Diana

Burglen, Lydie
License Information

Text and Data Mining valid from 2019-03-01

Text and Data Mining valid from 2019-03-01

Version of Record valid from 2022-01-19
More Information

This article is maintained by: Elsevier

Article Title: Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0089-2

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics

Document is current

Any future updates will be listed below