Incontinentia Pigmenti
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-54779-0_6
Reference35 articles.
1. Aradhya S, Woffendin H, Jakins T, Bardaro T, Esposito T, Smahi A, et al. 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(19):2171–9.
2. Maubach G, Schmadicke AC, Naumann M. NEMO links nuclear factor-kappaB to human diseases. Trends Mol Med. 2017;23:1138–55. Trends Mol Med 2018;24(7):654
3. Muller K, Courtois G, Ursini MV, Schwaninger M. New insight into the pathogenesis of cerebral small-vessel diseases. Stroke. 2017;48(2):520–7.
4. Alshenqiti A, Nashabat M, AlGhoraibi H, Tamimi O, Alfadhel M. Pulmonary hypertension and vasculopathy in incontinentia pigmenti: a case report. Ther Clin Risk Manag. 2017;13:629–34.
5. Fusco F, Pescatore A, Steffann J, Royer G, Bonnefont JP, Ursini MV. Clinical utility gene card for: incontinentia pigmenti. Eur J Hum Genet. 2013;21:7.
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