Nonsynonimous mutation of catechol-O-methyl-transferase (COMT) gene in a patient with temporomandibular disorder(483 views) D'Antò V, Michelotti A, Esposito L, Zagari A, Liguori R, Sacchetti L
J Sci Med Sport (ISSN: 1440-2440), 2010; 13(6): 174-179.
Keywords: Comt Gene, Disc Displacement Without Reduction, Mutation, Pain Sensitivity, Temporomandibular Joint Disorders, Catechol Methyltransferase, Genomic Dna, Adult, Article, Case Report, Clinical Assessment, Crystallography, Dna Sequence, Female, Gene Expression, Gene Mutation, Human, Jaw Disease, Masticatory Muscle, Myofascial Pain, Nociception, Nuclear Magnetic Resonance Imaging, Pain Assessment, Visual Analog Scale, Adenine, Agents Interacting With Transmitter, Hormone Or Drug Receptors, Arginine, Cytosine, Serine, Codon, Dislocation, Genetics, Joint Characteristics And Functions, Pathology, Physiology, Catechol O-Methyltransferase, Neurotransmitter Agents, Pain Measurement, Range Of Motion, Articular, Temporomandibular Joint Dysfunction Syndrome,
Affiliations: *** IBB - CNR ***
Department of Oral and Maxillofacial Surgery, University of Naples Federico II, Italy
Institute of biostructure and bioimaging, CNR, Naples, Italy
CEINGE Biotecnologie Avanzate S.C.a R.L, Naples, Italy
Department of Biochemistry and Medical Biotechnology, University of Naples Federico II, Italy
References: Not available.
Nonsynonimous mutation of catechol-O-methyl-transferase (COMT) gene in a patient with temporomandibular disorder