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Article

Two novel mutations in SCN1A gene in Iranian patients with epilepsy.

Archives of medical research - 1 Apr 2010

Ebrahimi Ahmad, Houshmand Massoud, Tonekaboni Seyed Hassan, Fallah Mahboob Passand Mohammd Sadegh, Zainali Sirous, Moghadasi Mehdi

Abstract excerpt

BACKGROUND AND AIMS: Epilepsy as a common chronic neurological disorder is characterized by recurrent unprovoked seizures. Febrile seizures are the most common type of epilepsy in infants and children. Our aim was the molecular analysis of SCN1A gene in affected Iranian patients with GEFS+ and Dravet syndrome diagnosed clinically to explain genotype-phenotype correlation and exact classification. METHODS: The 34...

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Source

Identifiers

PMID: 20682179
DOI: 10.1016/j.arcmed.2010.04.007

Genes

ABCB1
MTHFR

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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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