Electroencephalographic findings in KBG syndrome: a child...

Acta Neurologica Belgica 2015 / 12 Vol. 115; Iss. 4

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

Samanta, Debopam, Willis, Erin
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Volume:
115
Language:
english
Journal:
Acta Neurologica Belgica
DOI:
10.1007/s13760-014-0413-9
Date:
December, 2015
File:
PDF, 802 KB
english, 2015
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