Kleefstra-variant syndrome with heterozygous mutations in EHMT1 and KCNQ2 genes: a case report.

Giovanna MarcheseFrancesca RizzoAnna GuacciAlessandro WeiszGiangennaro Coppola

Published in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2016)

Keyphrases

early onset
genome wide
case report
bioinformatics analysis
genome wide identification
dna methylation
transcription factor