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Article

Copy number variations in Saudi family with intellectual disability and epilepsy.

BMC genomics - 17 Oct 2016

Naseer Muhammad I, Chaudhary Adeel G, Rasool Mahmood, Kalamegam Gauthaman, Ashgan Fai T, Assidi Mourad, Ahmed Farid, Ansari Shakeel A, Zaidi Syed Kashif, Jan Mohammed M, Al-Qahtani Mohammad H

Abstract excerpt

BACKGROUND: Epilepsy is genetically complex but common brain disorder of the world affecting millions of people with almost of all age groups. Novel Copy number variations (CNVs) are considered as important reason for the numerous neurodevelopmental disorders along with intellectual disability and epilepsy. DNA array based studies contribute to explain a more severe clinical presentation of the disease but...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 27766957
DOI: 10.1186/s12864-016-3091-6
PMCID: PMC5073808

Genes

CSMD1
DDT
DDTL
HPR

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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