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Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.

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CMTX3

Introduction

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

References

References

  1. ↑ “Entrez Gene: Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant)”.
Further reading

Further reading

  • Brewer M, Changi F, Antonellis A, Fischbeck K, Polly P, Nicholson G, Kennerson M (July 2008). “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. doi:10.1007/s10048-008-0126-4. PMID 18458969.
  • Hahn AF, Brown WF, Koopman WJ, Feasby TE (October 1990). “X-linked dominant hereditary motor and sensory neuropathy”. Brain. 113 ( Pt 5) (5): 1511–25. doi:10.1093/brain/113.5.1511. PMID 2245309.
  • Huttner IG, Kennerson ML, Reddel SW, Radovanovic D, Nicholson GA (December 2006). “Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth disease”. Neurology. 67 (11): 2016–21. doi:10.1212/01.wnl.0000247271.40782.b7. PMID 17159110.