Uncovering incontinentia pigmenti: From DNA sequence to pathophysiology
Incontinentia pigmenti (IP) is an X-linked dominant genodermatosis. The disease is known to be caused by recurrent deletion of exons 4–10 of the Inhibitor Of Nuclear Factor Kappa B Kinase Regulatory Subunit Gamma (IKBKG) gene located at the Xq28 chromosomal region, which encodes for NEMO/IKKgamma, a...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Published: |
Frontiers Research Foundation
2022
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| Online Access: | http://psasir.upm.edu.my/id/eprint/102528/ https://www.frontiersin.org/articles/10.3389/fped.2022.900606/full |
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