Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxia
Jean‐Marie Ravel, Mehdi Benkirane, Nadège Calmels, Cécilia Marelli, Fabienne Ory‐Magne, Claire Ewenczyk, Yosra Halleb, François Tison, Claire Lecocq, Guillaume Pisché, Philippe Casenave, Annabelle Chaussenot, Solène Frismand, Louise Tyvaert, Lise Larrieu, Morgane Pointaux, Nathalie Drouot, Carine Bossenmeyer‐Pourié, Abderrahim Oussalah, Jean‐Louis Guéant, Bruno Leheup, Céline Bonnet, Mathieu Anheim, Christine Tranchant, Laëtitia Lambert, Jamel Chelly, Michel Kœnig, M. Renaud
Topics & Concepts
DystoniaAtaxiaCerebellar ataxiaCognitive declineParkinsonismMedicinePediatricsGeneticsNeurosciencePsychologyBiologyPathologyDementiaDiseaseGenetic Neurodegenerative DiseasesGenomics and Rare DiseasesHereditary Neurological Disorders