Associated Papers
Novel homozygous mutations in Pakistani families with Charcot-Marie-Tooth disease.
Kanwal S et al.
Bmc Medical Genomics, 2021
Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster.
Gosselin I et al.
Neuromuscular Disorders : Nmd, 2008
A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypes.
Gooding R et al.
Journal of Medical Genetics, 2005
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