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Li, V. ERCC6 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5414 (accessed on 21 September 2026).
Li V. ERCC6 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5414. Accessed September 21, 2026.
Li, Vivi. "ERCC6 Gene" Encyclopedia, https://encyclopedia.pub/entry/5414 (accessed September 21, 2026).
Li, V. (2020, December 24). ERCC6 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5414
Li, Vivi. "ERCC6 Gene." Encyclopedia. Web. 24 December, 2020.
ERCC6 Gene
Edit

ERCC excision repair 6, chromatin remodeling factor

genes

References

  1. Horibata K, Iwamoto Y, Kuraoka I, Jaspers NG, Kurimasa A, Oshimura M,Ichihashi M, Tanaka K. Complete absence of Cockayne syndrome group B gene productgives rise to UV-sensitive syndrome but not Cockayne syndrome. Proc Natl Acad SciU S A. 2004 Oct 26;101(43):15410-5.
  2. Laugel V, Dalloz C, Durand M, Sauvanaud F, Kristensen U, Vincent MC, Pasquier L, Odent S, Cormier-Daire V, Gener B, Tobias ES, Tolmie JL, Martin-Coignard D,Drouin-Garraud V, Heron D, Journel H, Raffo E, Vigneron J, Lyonnet S, Murday V,Gubser-Mercati D, Funalot B, Brueton L, Sanchez Del Pozo J, Muñoz E, Gennery AR, Salih M, Noruzinia M, Prescott K, Ramos L, Stark Z, Fieggen K, Chabrol B, SardaP, Edery P, Bloch-Zupan A, Fawcett H, Pham D, Egly JM, Lehmann AR, Sarasin A,Dollfus H. Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved inCockayne syndrome. Hum Mutat. 2010 Feb;31(2):113-26. doi: 10.1002/humu.21154.
  3. Laugel V. Cockayne Syndrome. 2000 Dec 28 [updated 2019 Aug 29]. In: Adam MP,Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors.GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle;1993-2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK1342/
  4. Laugel V. Cockayne syndrome: the expanding clinical and mutational spectrum.Mech Ageing Dev. 2013 May-Jun;134(5-6):161-70. doi: 10.1016/j.mad.2013.02.006.
  5. Licht CL, Stevnsner T, Bohr VA. Cockayne syndrome group B cellular andbiochemical functions. Am J Hum Genet. 2003 Dec;73(6):1217-39.Review.
  6. Newman JC, Bailey AD, Weiner AM. Cockayne syndrome group B protein (CSB) playsa general role in chromatin maintenance and remodeling. Proc Natl Acad Sci U S A.2006 Jun 20;103(25):9613-8.
  7. Spivak G, Hanawalt PC. Host cell reactivation of plasmids containing oxidativeDNA lesions is defective in Cockayne syndrome but normal in UV-sensitive syndromefibroblasts. DNA Repair (Amst). 2006 Jan 5;5(1):13-22.
  8. Vélez-Cruz R, Egly JM. Cockayne syndrome group B (CSB) protein: at thecrossroads of transcriptional networks. Mech Ageing Dev. 2013May-Jun;134(5-6):234-42. doi: 10.1016/j.mad.2013.03.004.
  9. Wilson BT, Lochan A, Stark Z, Sutton RE. Novel missense mutations in aconserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights intoCockayne syndrome. Am J Med Genet A. 2016 Mar;170(3):773-6. doi:10.1002/ajmg.a.37501.
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Update Date: 24 Dec 2020
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