The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia...
The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti
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Publisher
Switzerland: MDPI AG
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Language
English
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Publisher
Switzerland: MDPI AG
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Contents
Incontinentia pigmenti (IP) is a rare skin disease combined with anomalies of the teeth, eyes, and central nervous system (CNS). Mutations of the
gene are responsible for IP. Among the most frequent CNS abnormalities found in IP using magnetic resonance imaging (MRI) are corpus callosum (CC) abnormalities. The aim of the study was to determine t...
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Full title
The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti
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TN_cdi_doaj_primary_oai_doaj_org_article_581be68129d3486197b88ad4ca2d5e9d
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_581be68129d3486197b88ad4ca2d5e9d
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ISSN
2075-4418
E-ISSN
2075-4418
DOI
10.3390/diagnostics13071300
