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IKBKG mutation with incontinentia pigmenti and ring-enhancing encephalopathy
Journal article   Open access

IKBKG mutation with incontinentia pigmenti and ring-enhancing encephalopathy

D. Eksambe, N. Agim, N. Uddin, G. Gotway and J. M. Pascual
JAMA Neurology, Vol.72(12)
2015
DOI: https://doi.org/10.1001/jamaneurol.2015.2795

Abstract

alanine aminotransferase aspartate aminotransferase glucose immunoglobulin enhancer binding protein kappa beta kinase gamma gene protein unclassified drug I kappa B kinase IKBKG protein, human alanine aminotransferase blood level aspartate aminotransferase blood level blood culture brain disease case report cerebrospinal fluid analysis DNA sequence erythema female gene deletion gene mutation glucose blood level Herpes simplex virus histopathology human incontinentia pigmenti infant infection Letter nuclear magnetic resonance imaging ophthalmoscopy polymerase chain reaction priority journal protein cerebrospinal fluid level ring enhancing encephalopathy virus culture complication genetics metabolism mutation pathology retina Alanine Transaminase Aspartate Aminotransferases Brain Diseases Humans I-kappa B Kinase
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https://doi.org/10.1001/jamaneurol.2015.2795View
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