Protein X-vezane dominantne Charcot-Marie-Toothove neuropatije 3 je protein koji je kod ljudi kodiran genom CMTX3.[2]
Dopunska literatura
uredi
- Brewer M, Changi F, Antonellis A, Fischbeck K, Polly P, Nicholson G, Kennerson M (juli 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. PMC 6852654. PMID 18458969.
- Hahn AF, Brown WF, Koopman WJ, Feasby TE (oktobar 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 (decembar 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.