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Journal of the Formosan Medical Association
Volume 109, Issue 3
, Pages 192-200
, March 2010
NEMO Gene Mutations in Chinese Patients With Incontinentia Pigmenti
References
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- Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium . Nature . 2000;405:466–472
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- Genetic approaches in mice to understand Rel/NF-kappaB and IkappaB function: transgenics and knockouts . Oncogene . 1999;18:6888–6895
- A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations . Hum Mol Genet . 2001;10:2171–2179
- Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-kappaB activation . Hum Mol Genet . 2004;13:1763–1773
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PII: S0929-6646(10)60042-3
doi: 10.1016/S0929-6646(10)60042-3
© 2010 Formosan Medical Association & Elsevier. Published by Elsevier Inc. All rights reserved.
« Previous
Next »
Journal of the Formosan Medical Association
Volume 109, Issue 3
, Pages 192-200
, March 2010
