CMTX3

CMTX3
Identifiers
Aliases CMTX3
External IDs GeneCards: CMTX3
Orthologs
Species Human Mouse
Entrez

1254

n/a

Ensembl

n/a

n/a

UniProt

n/a

n/a

RefSeq (mRNA)

NM_000392

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC) n/a n/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)". Retrieved 2014-02-23.

Further reading

  • Brewer, M; Changi, F; Antonellis, A; Fischbeck, K; Polly, P; Nicholson, G; Kennerson, M (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, A. F.; Brown, W. F.; Koopman, W. J.; Feasby, T. E. (1990). "X-linked dominant hereditary motor and sensory neuropathy". Brain : a journal of neurology. 113 (5): 1511–25. doi:10.1093/brain/113.5.1511. PMID 2245309. 
  • Huttner, I. G.; Kennerson, M. L.; Reddel, S. W.; Radovanovic, D; Nicholson, G. A. (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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