CMTX3 explained

Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) is a protein that in humans is encoded by the CMTX3 gene.^[1]

Further reading

• Brewer M, Changi F, Antonellis A, Fischbeck K, Polly P, Nicholson G, Kennerson M . Evidence of a founder haplotype refines the X-linked Charcot-Marie-Tooth (CMTX3) locus to a 2.5 Mb region . Neurogenetics . 9 . 3 . 191–5 . July 2008 . 18458969 . 10.1007/s10048-008-0126-4 . 6852654 .
• Hahn AF, Brown WF, Koopman WJ, Feasby TE . X-linked dominant hereditary motor and sensory neuropathy . Brain . 113 (Pt 5) . 5 . 1511–25 . October 1990 . 2245309 . 10.1093/brain/113.5.1511 .
• Huttner IG, Kennerson ML, Reddel SW, Radovanovic D, Nicholson GA . Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth disease . Neurology . 67 . 11 . 2016–21 . December 2006 . 17159110 . 10.1212/01.wnl.0000247271.40782.b7 . 11583264 .

Notes and References

1. Web site: Entrez Gene: Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) .