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Li, V. DCX Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4535 (accessed on 28 September 2026).
Li V. DCX Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4535. Accessed September 28, 2026.
Li, Vivi. "DCX Gene" Encyclopedia, https://encyclopedia.pub/entry/4535 (accessed September 28, 2026).
Li, V. (2020, December 23). DCX Gene. In Encyclopedia. https://encyclopedia.pub/entry/4535
Li, Vivi. "DCX Gene." Encyclopedia. Web. 23 December, 2020.
DCX Gene
Edit

Doublecortin: The DCX gene provides instructions for producing a protein called doublecortin. 

genes

References

  1. Bahi-Buisson N, Souville I, Fourniol FJ, Toussaint A, Moores CA, Houdusse A,Lemaitre JY, Poirier K, Khalaf-Nazzal R, Hully M, Leger PL, Elie C, Boddaert N,Beldjord C, Chelly J, Francis F; SBH-LIS European Consortium. New insights intogenotype-phenotype correlations for the doublecortin-related lissencephalyspectrum. Brain. 2013 Jan;136(Pt 1):223-44. doi: 10.1093/brain/aws323.
  2. Friocourt G, Marcorelles P, Saugier-Veber P, Quille ML, Marret S, Laquerrière A. Role of cytoskeletal abnormalities in the neuropathology and pathophysiologyof type I lissencephaly. Acta Neuropathol. 2011 Feb;121(2):149-70. doi:10.1007/s00401-010-0768-9.
  3. Fry AE, Cushion TD, Pilz DT. The genetics of lissencephaly. Am J Med Genet CSemin Med Genet. 2014 Jun;166C(2):198-210. doi: 10.1002/ajmg.c.31402.
  4. González-Morón D, Vishnopolska S, Consalvo D, Medina N, Marti M, Córdoba M,Vazquez-Dusefante C, Claverie S, Rodríguez-Quiroga SA, Vega P, Silva W, Kochen S,Kauffman MA. Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders. PLoS One. 2017Sep 27;12(9):e0185103. doi: 10.1371/journal.pone.0185103.
  5. Liu JS. Molecular genetics of neuronal migration disorders. Curr NeurolNeurosci Rep. 2011 Apr;11(2):171-8. doi: 10.1007/s11910-010-0176-5. Review.
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Update Date: 23 Dec 2020
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