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Article

Nonsynonimous mutation of catechol-O-methyl-transferase (COMT) gene in a patient with temporomandibular disorder.

Progress in orthodontics - 1 Jan 2010

D'Antò Vincenzo, Michelotti Ambrosina, Esposito Luciana, Zagari Adriana, Liguori Rosario, Sacchetti Lucia

Abstract excerpt

We report a case of temporomandibular disorder patient with disc displacement without reduction, myofascial pain, limited opening and a novel, never described, nonsynonimous mutation of catechol-O-methyl-transferase (COMT) gene. COMT is one of the enzymes that metabolizes catecholamines, thereby...

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Source

Identifiers

PMID: 20974455
DOI: 10.1016/j.pio.2010.09.007

Genes

COMT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-20974455-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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