Research Article

High carriers frequency of an apparently ancient founder mutation p.Tyr322X in the ERCC8 gene responsible for Cockayne syndrome among Christian Arabs in Northern Israel†

  1. Morad Khayat1,
  2. Hagar Hardouf1,
  3. Joel Zlotogora2,
  4. Stavit Allon Shalev1,3,*

Article first published online: 24 NOV 2010

DOI: 10.1002/ajmg.a.33746

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 152A, Issue 12, pages 3091–3094, December 2010

Additional Information

How to Cite

Khayat, M., Hardouf, H., Zlotogora, J. and Shalev, S. A. (2010), High carriers frequency of an apparently ancient founder mutation p.Tyr322X in the ERCC8 gene responsible for Cockayne syndrome among Christian Arabs in Northern Israel. Am. J. Med. Genet., 152A: 3091–3094. doi: 10.1002/ajmg.a.33746

Author Information

  1. 1

    Genetics Institute, Ha'Emek Medical Center, Afula, Israel

  2. 2

    Department of Community Genetics, Public Health Services, Ministry of Health, Hebrew University Jerusalem, Jerusalem, Israel

  3. 3

    Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel

*Genetics Institute, Ha'Emek Medical Center, Afula 18101, Israel.

  1. †

    How to Cite this Article: Khayat M, Hardouf H, Zlotogora J, Shalev SA. 2010. High carriers frequency of an apparently ancient founder mutation p.Tyr322X in the ERCC8 gene responsible for Cockayne syndrome among Christian Arabs in Northern Israel. Am J Med Genet Part A 152A:3091–3094.

Publication History

  1. Issue published online: 24 NOV 2010
  2. Article first published online: 24 NOV 2010
  3. Manuscript Accepted: 16 SEP 2010
  4. Manuscript Received: 27 JUL 2010

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