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Article

IKBKG Mutation With Incontinentia Pigmenti and Ring-Enhancing Encephalopathy.

JAMA neurology - 1 Dec 2015

Eksambe Deepali, Agim Nnenna, Uddin Naseem, Gotway Garrett, Pascual Juan M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 26658971
DOI: 10.1001/jamaneurol.2015.2795

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IKBKG Mutation With Incontinentia Pigmenti and Ring-Enhancing Encephalopathy.PMID 26658971Read ↗

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Incontinentia Pigmenti: A Comprehensive Review and Update.Semantic proximity Read ↗

Alterations of the IKBKG locus and diseases: an update and a report of 13 novel mutations.Semantic proximity Read ↗

Diagnostic and molecular genetic challenges in male incontinentia pigmenti: a case report.Semantic proximity Read ↗

Incontinentia pigmenti with retinal vascular anomaly and deletion of exons 4-10 in NEMO.Semantic proximity Read ↗

Incontinetia pigmenti-related myopathy or unsolved "double trouble"?Semantic proximity Read ↗

Unusual Father-to-Daughter Transmission of Incontinentia Pigmenti Due to Mosaicism in IP MalesSemantic proximity Read ↗

Importance of extracutaneous organ involvement in determining the clinical severity and prognosis of incontinentia pigmenti caused by mutations in the IKBKG gene.Semantic proximity Read ↗

Incontinentia pigmenti: the first single gene disorder due to disrupted NF-kappa B function.Semantic proximity Read ↗

A novel IKBKG mutation in a patient with incontinentia pigmenti and features of hepatic ciliopathy.Semantic proximity Read ↗

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