CMTX3
{{Short description|Protein-coding gene in humans}}
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Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) is a protein that, in humans, is encoded by the CMTX3 gene.{{cite web | title = Entrez Gene: Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) | url = https://www.ncbi.nlm.nih.gov/gene/1254 }}
References
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Further reading
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- {{cite journal | vauthors = Brewer M, Changi F, Antonellis A, Fischbeck K, Polly P, Nicholson G, Kennerson M | title = Evidence of a founder haplotype refines the X-linked Charcot-Marie-Tooth (CMTX3) locus to a 2.5 Mb region | journal = Neurogenetics | volume = 9 | issue = 3 | pages = 191–5 | date = July 2008 | pmid = 18458969 | doi = 10.1007/s10048-008-0126-4 | pmc = 6852654 }}
- {{cite journal | vauthors = Hahn AF, Brown WF, Koopman WJ, Feasby TE | title = X-linked dominant hereditary motor and sensory neuropathy | journal = Brain | volume = 113 ( Pt 5) | issue = 5 | pages = 1511–25 | date = October 1990 | pmid = 2245309 | doi = 10.1093/brain/113.5.1511 }}
- {{cite journal | vauthors = Huttner IG, Kennerson ML, Reddel SW, Radovanovic D, Nicholson GA | title = Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth disease | journal = Neurology | volume = 67 | issue = 11 | pages = 2016–21 | date = December 2006 | pmid = 17159110 | doi = 10.1212/01.wnl.0000247271.40782.b7 | s2cid = 11583264 }}
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