Behavioral and Molecular Exploration of the AR-CMT2A Mouse Model Lmna R298C/R298C

Lamines A et syndromes progéroïdes

(2011) Claire L. Navarro et al.   M S-MEDECINE SCIENCES

Sensorimotor and cognitive function of a NEFLP22S mutant model of Charcot–Marie–Tooth disease type 2E

(2010) Mohammed Filali et al.   BEHAVIOURAL BRAIN RESEARCH

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

(2010) H. Skre   CLINICAL GENETICS

Update on Charcot-Marie-Tooth Disease

(2010) Ágnes Patzkó et al.   Current Neurology and Neuroscience Reports

Foot pad skin biopsy in mouse models of hereditary neuropathy

(2010) Patrizia Dacci et al.   GLIA

Reversal of neuropathy phenotypes in conditional mouse model of Charcot–Marie–Tooth disease type 2E

(2010) Florence Dequen et al.   HUMAN MOLECULAR GENETICS

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy

(2009) F. Achilli et al.   Disease Models & Mechanisms

Charcot–Marie–Tooth disease

(2009) Kinga Szigeti et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

An Update on Nerve Biopsy

(2009) Jean-Michel Vallat et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

A Cardio-Neurological Form of Laminopathy: Dilated Cardiomyopathy with Permanent Partial Atrial Standstill and Axonal Neuropathy

(2009) ALEXANDRE DUPARC et al.   PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY

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

(2008) T. Hamadouche et al.   ANNALS OF HUMAN GENETICS