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Article

Neuropathology of 16p13.11 deletion in epilepsy.

PloS one - 1 Jan 2012

Liu Joan Y W, Kasperavičiūtė Dalia, Martinian Lillian, Thom Maria, Sisodiya Sanjay M

Abstract excerpt

16p13.11 genomic copy number variants are implicated in several neuropsychiatric disorders, such as schizophrenia, autism, mental retardation, ADHD and epilepsy. The mechanisms leading to the diverse clinical manifestations of deletions and duplications at this locus are unknown. Most studies favour NDE1 as the leading disease-causing candidate gene at 16p13.11. In epilepsy at least, the deletion does not appear...

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Source

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Identifiers

PMID: 22523559
DOI: 10.1371/journal.pone.0034813
PMCID: PMC3327721

Genes

NDE1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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