Biology:CMTX3
From HandWiki
Short description: Protein-coding gene in humans
 Generic protein structure example |
Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) is a protein that in humans is encoded by the CMTX3 gene.[1]
References
Further reading
- "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. doi:10.1007/s10048-008-0126-4. PMID 18458969.
- "X-linked dominant hereditary motor and sensory neuropathy". Brain 113 ( Pt 5) (5): 1511–25. October 1990. doi:10.1093/brain/113.5.1511. PMID 2245309.
- "Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth disease". Neurology 67 (11): 2016–21. December 2006. doi:10.1212/01.wnl.0000247271.40782.b7. PMID 17159110.
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