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Clinical, biomarker, and molecular delineations and genotype-Phenotype correlations of ataxia with oculomotor apraxia type 1
Mathilde Renaud, Maria Céu Moreira, Bondo Ben Monga, Diana Rodriguez, Rabab Debs, Perrine Charles, Malika Chaouch, Farida Ferrat, Chloé Laurencin, Laurent Vercueil, Martial Mallaret, Abderrahim M’Zahem, Lamia Ali Pacha, Meriem Tazir, Caroline Tilikete, Elisabeth Ollagnon, François Ochsner, Thierry Kuntzer, Hans H. Jung, Jean Marie Beis
*Corresponding author for this work
- Université de Strasbourg
- Université de Lubumbashi
- Hôpital d'Enfants Armand Trousseau
- Sorbonne Université
- Institut national de la santé et de la recherche médicale
- Etablissement Hospitalier Spécialisé
- University of Algiers Benyoucef Benkhedda
- Universite Claude Bernard Lyon 1
- CNRS
- CHU de Grenoble
- Center de Recherche U836
- CHU Constantine
- University Hospital Center Mustapha Pasha
- Hôpital neurologique et neurochirurgical Pierre Wertheimer
- Hospices civils de Lyon
- University of Lausanne
- University of Zurich
- Centre de Lay-Saint-Christophe
- Centre Hospitalier de Bigorre
- Innsbruck Medical University
- University of Minnesota Twin Cities
- University of Geneva
- Trinity College Dublin
- Trinity College Dublin
- Department of Public Health and Environment
- CHU de Toulouse
- Pediatric Neurology
- University of Amsterdam
- Universidade de São Paulo
- Universidade Federal do Rio Grande do Sul
- Schneider Childrens Medical Center Israel
- Assistance publique – Hôpitaux de Paris
- Assistance publique - Hôpitaux de Marseille
- Université de Montpellier
- Bordeaux University Hospital
- Université de Bordeaux
Research output: Contribution to journal › Article › peer-review
30
Scopus
citations