Ataxie avec apraxie oculomotrice de type 2 (AOA2) : étude clinique, biologique et corrélation génotype/phénotype d’une cohorte de 90 patients

Anheim, Mathieu; Monga, Ben; Fleury, Marie-Céline; Charles, P Peterson; Barbot, Clara; Salih, Mustafa A.; Delaunoy, Jean-Louis; Fritsch, M.; Arning, Larissa; Synofzik, Matthis; Schöls, Lüdger; Sequeiros, Jorge; Goizet, Cyril; Marelli, Cécilia; Ber, Isabelle Le; Koht, Jeanette; Gazulla, José; Bleecker, Jan De; Mukhtar, Maowia M.; Drouot, Nathalie; Alipacha, Lamia; Benhassine, Traki; Chbiche, M.; M’zahem, A.; Hamri, Abdelmajid; Chabrol, B.; Pouget, Jean; Murphy, Ronan P.; Watanabe, Masao; Coutinho, Paula; Tazir, Mériem; Dürr, Alfred; Brice, Alexis; Tranchant, C.; Koenig, Michael L.

doi:10.1016/s0035-3787(10)70006-0

Revue Neurologique

2010

DOI: 10.1016/s0035-3787(10)70006-0

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Ataxie avec apraxie oculomotrice de type 2 (AOA2) : étude clinique, biologique et corrélation génotype/phénotype d’une cohorte de 90 patients

Mathieu Anheim

Ben Monga

Marie-Céline Fleury

et al.

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Ataxie avec apraxie oculomotrice de type 2 (AOA2) : étude clinique, biologique et corrélation génotype/phénotype d’une cohorte de 90 patients

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