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Article

Assessing the relative incidence of mitochondrial DNA A3243G in migraine without aura with maternal inheritance.

Headache - 1 Jan 2000

Di Gennaro G, Buzzi M G, Ciccarelli O, Santorelli F M, Pierelli F, Fortini D, D'Onofrio M, Costa A, Nappi G, Casali C

Abstract excerpt

OBJECTIVE: To determine whether patients with migraine without aura with maternal "inheritance" are affected by a monosymptomatic form of the MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes) or carry the most common mitochondrial DNA (mtDNA) mutation associated with MELAS, namely the A3243G transition in the transfer RNA (tRNA)Leu(UUR) gene. BACKGROUND: The association...

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Identifiers

PMID: 10940095
DOI: 10.1046/j.1526-4610.2000.00088.x

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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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