| CMTX3 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | CMTX3, Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | GeneCards: CMTX3; OMA: CMTX3 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) is a protein that in humans is encoded by the CMTX3 gene. [2]
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 Wikipedia by expanding it. |
| CMTX3 | |||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | CMTX3, Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | GeneCards: CMTX3; OMA: CMTX3 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) is a protein that in humans is encoded by the CMTX3 gene. [2]
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.
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| This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by expanding it. |