Incontinentia pigmenti in adults
Author:
Affiliation:
1. Department of Pediatrics, Division of Genetics and MetabolismUniversity of Texas Southwestern Medical Center Dallas Texas
Funder
University of Texas Southwestern Medical Center
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61205
Reference22 articles.
1. A recurrent deletion in the ubiquitously expressed NEMO (IKK‐gamma) gene accounts for the vast majority of incontinentia pigmenti mutations;Aradhya S.;Human Molecular Genetics,2001
2. The two NF‐kappaB activation pathways and their role in innate and adaptive immunity;Bonizzi G.;Trends in Immunology,2004
3. Incontinentia pigmenti: report on data from 2000 to 2013;Fusco F.;Orphanet Journal of Rare Diseases,2014
4. EDA‐ID and IP, two facies of the same coin: How the same IKBKG/NEMO mutation affecting the NF‐kB pathway can cause immunodeficiency and/or inflammation;Fusco F.;International Reviews of Immunology,2015
5. Peculiar pigmentation of the skin in an infant;Garrod A. E.;Teansaction The Clinical Society London,1906
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1. Bioinformatic Analysis of IKK Complex Genes Expression in Selected Gastrointestinal Cancers;International Journal of Molecular Sciences;2024-09-12
2. A case report of neonatal incontinentia pigmenti complicated by severe cerebrovascular lesions in one of the male monozygotic twins;Frontiers in Pediatrics;2024-05-21
3. Neurocutaneous disorders;Neurogenetics for the Practitioner;2024
4. A case report of neonatal incontinentia pigmenti complicated by severe cerebrovascular lesions in one of the male monozygotic twins;2023-09-11
5. Uncovering incontinentia pigmenti: From DNA sequence to pathophysiology;Frontiers in Pediatrics;2022-09-06
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