CMTX2
| CMTX2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | CMTX2, Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive) | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | GeneCards: CMTX2; OMA:CMTX2 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive) is a protein that in humans is encoded by the CMTX2 gene.[2] Its cytogenetic location is Xp22.2.[3] It is associated with a variant of Charcot-Marie-Tooth disease.[2]
References
[edit]- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ a b "Entrez Gene: Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)". Retrieved 2014-02-23.
- ^ "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2; CMTX2". Online Mendelian Inheritance in Man. Retrieved 2024-10-17.
Further reading
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