A genetic cause for neonatal encephalopathy: Incontinentia pigmenti with NEMO mutation

Acta Paediatrica, International Journal of Paediatrics

Volumn 97, Issue 3, 2008, Pages 379-381

  Loh, Ne Ron ^a   Jadresic, Lyda P ^a   Whitelaw, Andrew ^b  

^a GLOUCESTERSHIRE ROYAL HOSPITAL   (United Kingdom)

^b UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

Apoptosis; Incontinentia pigmenti; Inflammation; NEMO mutation; Neonatal encephalopathy

Indexed keywords

ARTICLE; BASAL GANGLION; BRAIN DISEASE; CASE REPORT; DELIVERY; FEMALE; GENE; GENE MUTATION; HISTOLOGY; HUMAN; HUMAN TISSUE; INCONTINENTIA PIGMENTI; INFANT; NEMO GENE; PRIORITY JOURNAL; RASH; WHITE MATTER;

APOPTOSIS; BRAIN DISEASES; FEMALE; HUMANS; I-KAPPA B KINASE; INCONTINENTIA PIGMENTI; INFANT, NEWBORN; MUTATION;

EID: 41949110079     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2007.00630.x     Document Type: Article

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