CMTX3

CMTX3
Identifiers
AliasesCMTX3, Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant)
External IDsGeneCards: CMTX3
Orthologs
SpeciesHumanMouse
Entrez

1254

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed search[1]n/a
Wikidata
View/Edit Human

Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) is a protein that in humans is encoded by the CMTX3 gene.[2]

References

  1. ↑ "Human PubMed Reference:".
  2. ↑ "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. 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.
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