NEMO gene mutations in Chinese patients with incontinentia pigmenti.

@article{Hsiao2010NEMOGM,
  title={NEMO gene mutations in Chinese patients with incontinentia pigmenti.},
  author={P. H. Hsiao and S. -F. Lin and Shu-Shien Chiang and Yu-Hung Wu and H. Chen and Yang-Chih Lin},
  journal={Journal of the Formosan Medical Association = Taiwan yi zhi},
  year={2010},
  volume={109 3},
  pages={192-200}
}
BACKGROUND/PURPOSE Incontinentia pigmenti is a rare, X-linked, dominant genodermatosis affecting skin, teeth, eyes, and central nervous system. Symptoms are associated with mutations in the nuclear factor-kappa B essential modulator (NEMO) gene on chromosome Xq28. Here, a subpopulation of Chinese patients with incontinentia pigmenti were examined to investigate the frequency and pattern of NEMO mutations, and to analyze their clinical features. METHODS From January 1996 to August 2006, 52… CONTINUE READING

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[An incontinentia pigmenti family with deletion in both NEMO gene and pseudogene DeltaNEMO].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics • 2008

A case report of incontinentia pigmenti

XF Zhang, Y. Li
Zhongguo Dang Dai Er Ke Za Zhi 2007;9:503–4 • 2007

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