E. Le Guern

GABA_AReceptor γ2 Subunit Mutations Linked to Human Epileptic Syndromes Differentially Affect Phasic and Tonic Inhibition

Emmanuel Eugène, Christel Depienne, Stéphanie Baulac et al. · Journal of Neuroscience · 2007 · 83 citations · Full text

Characterization of Recessive Parkinson Disease in a Large Multicenter Study

Suzanne Lesage, Ariane Lunati, Marion Houot et al. · Annals of Neurology · 2020 · 77 citations · Full text

Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene

Nazha Birouk, Hamid Azzedine, O. Dubourg et al. · Archives of Neurology · 2003 · 76 citations

New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease

L.J. Bone, Niklas Dahl, M. William Lensch et al. · Neurology · 1995 · 69 citations

Molecular Diagnostic Techniques, Mendelian Disorder, Genetic Disorder +12

Autosomal‐dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I

Ali Benomar, E. Le Guern, Alexandra Dürr et al. · Annals of Neurology · 1994 · 65 citations