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Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 gene

Debopam Samanta1, Erin Willis2

  • 1Division of Child Neurology, University of Arkansas for Medical Sciences, 4301 West Markham Street, Little Rock, AR, 72205, USA. dsamanta@uams.edu.

Acta Neurologica Belgica
|December 29, 2014
PubMed
Abstract

No abstract available in PubMed .

Keywords:
ANKRD11 mutationCharacteristic EEGEpilepsyKBG syndrome

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