Nicolas Lacoste

Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons

H. Lochmüller, B. Eymard, E. Girard, 2022, Acta Neuropathologica.

New MORC2 gene mutations are associated with distinctive features: from axonal neuropathy to late adult-onset spinal muscular atrophy like phenotype

P. Latour, T. Stojkovic, A. Nadaj-Pakleza, 2022 .

Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy

P. Latour, T. Stojkovic, S. Allouche, 2022, Brain : a journal of neurology.

Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report

F. Bouhour, R. Froissart, M. Hermier, 2022, Genes.

H2A.Z is involved in premature aging and DSB repair initiation in muscle fibers

A. Hamiche, P. Mari, Edwige Belotti, 2024, Nucleic acids research.