NEMO Gene Mutations in Chinese Patients With Incontinentia Pigmenti
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference26 articles.
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2. Incontinentia pigmenti (BlochSulzberger syndrome);Landy;J Med Genet,1993
3. Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium;Smahi;Nature,2000
4. Control of apoptosis by Rel/ NF-kappaB transcription factors;Barkett;Oncogene,1999
5. Genetic approaches in mice to understand Rel/NF-kappaB and IkappaB function: transgenics and knockouts;Gerondakis;Oncogene,1999
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1. Central nervous system anomalies in 41 Chinese children incontinentia pigmenti;BMC Neuroscience;2024-05-21
2. Thrombocytosis and eosinophilia in 32 Chinese neonatal incontinentia pigmenti patients.;2022-09-09
3. Uncovering incontinentia pigmenti: From DNA sequence to pathophysiology;Frontiers in Pediatrics;2022-09-06
4. Late contralateral recurrence of retinal detachment in incontinentia pigmenti: A case report;World Journal of Clinical Cases;2022-05-06
5. Hypomorphic mutation of IKBKG in a male patient with incontinentia pigmenti;The Journal of Dermatology;2020-04
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