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Article

14q12 duplication including FOXG1: is there a common age-dependent epileptic phenotype?

Brain & development - 1 May 2014

Bertossi Chiara, Cassina Matteo, De Palma Luca, Vecchi Marilena, Rossato Sara, Toldo Irene, Donà Marta, Murgia Alessandra, Boniver Clementina, Sartori Stefano

Abstract excerpt

INTRODUCTION: Duplications of 14q12 encompassing FOXG1 gene have been recently associated with developmental delay, severe speech impairment, epilepsy, aspecific neuroimaging findings and minor dysmorphisms. AIM AND METHODS: In order to refine the epileptic phenotype associated with 14q12 duplications, we have performed a review of the electroclinical picture of the patients reported to date in the literature,...

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Source

Identifiers

PMID: 23838309
DOI: 10.1016/j.braindev.2013.06.008

Genes

FOXG1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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