D. Grid

Spine deformities in Charcot-Marie-Tooth 4C caused by <i>SH3TC2</i> gene mutations

Hamid Azzedine, N. Ravisé, Christophe Verny et al. · Neurology · 2006 · 104 citations

A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3

Ahmed Bouhouche, Ali Benomar, Nazha Birouk et al. · The American Journal of Human Genetics · 1999 · 88 citations · Full text

Mendelian Disorder, Cytogenetics, Genetic Disorder +7

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33

Éric Leguern, A. Guilbot, M. Kessali et al. · Neuromuscular Disorders · 1997 · 12 citations

Mendelian Disorder, Genetic Disorder, Charcot-marie-tooth Disease +9

The Autosomal Recessive Form of CMT Disease Linked to 5q31‐q33

A. Guilbot, M. Kessali, N. Ravisé et al. · Annals of the New York Academy of Sciences · 1999 · 10 citations

Mendelian Disorder, Genetic Disorder, Genetics +4