Uncovering incontinentia pigmenti: From DNA sequence to pathophysiology

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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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Bibliographic Details
Main Authors:	Kang, Nien How, Jing, Hazel Yi Leong, Dwi Pramono, Zacharias Aloysius, Kin, Fon Leong, Zee, Wei Lai, Wei, Hsum Yap
Format:	Article
Published:	Frontiers Research Foundation 2022
Online Access:	http://psasir.upm.edu.my/id/eprint/102528/

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