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Article

Neuronal migration disorders, genetics, and epileptogenesis.

Journal of child neurology - 1 Apr 2005

Guerrini Renzo, Filippi Tiziana

Abstract excerpt

Several malformation syndromes with abnormal cortical development have been recognized. Specific causative gene defects and characteristic electroclinical patterns have been identified for some. X-linked periventricular nodular heterotopia is mainly seen in female patients and is often associated with focal epilepsy. FLN1 mutations have been reported in all familial cases and in about 25% of sporadic patients. A...

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Identifiers

PMID: 15921228
DOI: 10.1177/08830738050200040401

Genes

DCX
ARX
EMX2
RELN

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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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