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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Frontiers Media S.A.,
2022-09-01T00:00:00Z.
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