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CMTX3

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Protein-coding gene in humans

CMTX3

Identifiers

CMTX3, Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant)

External IDs

GeneCards: CMTX3; OMA:CMTX3 - orthologs

Species

Human

Mouse


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RefSeq (mRNA)


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RefSeq (protein)


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Location (UCSC)

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PubMed search

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View/Edit Human

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

References

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant)".

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. PMC 6852654. 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. S2CID 11583264.

This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Misplaced Pages by expanding it.

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