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Article

Array-comparative genomic hybridization analysis of a cohort of Saudi patients with epilepsy.

CNS & neurological disorders drug targets - 1 Jan 2015

Faheem Muhammad, Naseer Muhammad I, Chaudhary Adeel G, Kumosani Taha A, Rasool Mahmood, Algahtani Hussein A, Bibi Fehmida, Kamal Mohammad A, Al-Qahtani Mohammad H

Abstract excerpt

Specific genetic anomalies or non-genetic factors could lead to epilepsy, but in various cases the underlying cause is unknown. Novel technologies, such as array comparative genomic hybridization, may reveal the copy number variants (CNVs), established as significant risk factor for epilepsy. This study carried out a high-density whole genome array- comparative genomic hybridization analysis with blood DNA...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25921748
DOI: 10.2174/1871527314666150429111737

Genes

CHRNA4
GABRG3
KCNQ2
NRXN3
PPDPF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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