Publisher: Karger
E-ISSN: 1424-859x|146|2|115-119
ISSN: 1424-8581
Source: Cytogenetic and Genome Research, Vol.146, Iss.2, 2015-08, pp. : 115-119
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Abstract
We report the first case of an 18p11.32 deletion, detected by array CGH, associated with a drug-resistant form of atypical absence epilepsy, global developmental delay and no signs of holoprosencephaly (HPE). In particular, this region encompasses 19 genes, and none of these genes have been strictly associated with epilepsy. Among these,
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