Nicolas Lévy

G.O.3 Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H

E. Chouery, A. Mégarbané, D. Grid, 2007, Neuromuscular Disorders.

Microsatellite instability and defects in mismatch repair proteins: a new aetiology for Sertoli cell-only syndrome.

D. Lamb, C. Niederberger, L. Lipshultz, 2003, Molecular human reproduction.

LMNA mutations in atypical Werner's syndrome

C. Vigouroux, A. Garg, J. Capeau, 2003, The Lancet.

Drug screening on Hutchinson Gilford progeria pluripotent stem cells reveals aminopyrimidines as new modulators of farnesylation

M. Peschanski, J. Tournois, X. Nissan, 2016, Cell Death and Disease.

Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot‐Marie‐Tooth Subtype CMT2B1 in Families from North Western Africa

E. Génin, N. Lévy, D. Grid, 2008, Annals of human genetics.