Format

Send to

Choose Destination
Acta Neurol Belg. 2015 Dec;115(4):779-82. doi: 10.1007/s13760-014-0413-9. Epub 2014 Dec 28.

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

Author information

1
Division of Child Neurology, University of Arkansas for Medical Sciences, 4301 West Markham Street, Little Rock, AR, 72205, USA. dsamanta@uams.edu.
2
Division of Child Neurology, University of Arkansas for Medical Sciences, 4301 West Markham Street, Little Rock, AR, 72205, USA.

KEYWORDS:

ANKRD11 mutation; Characteristic EEG; Epilepsy; KBG syndrome

PMID:
25543316
DOI:
10.1007/s13760-014-0413-9
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Springer
Loading ...
Support Center