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Catechol-O-methyltransferase Val158Met polymorphism and hyperactivity symptoms in Egyptian children with autism spectrum disorder
Faculty
Medicine
Year:
2013
Type of Publication:
ZU Hosted
Pages:
Authors:
Noha Abdel Halim Mohamed Rezk
Staff Zu Site
Abstract In Staff Site
Journal:
Research in Developmental Disabilities elsevier
Volume:
Keywords :
Catechol-O-methyltransferase Val158Met polymorphism and hyperactivity symptoms , Egyptian
Abstract:
Catechol-O-methyltransferase (COMT) plays an important role in the catabolism of brain dopamine and norepinephrine, which have been implicated in the pathogenesis of Autism spectrum disorder (ASD) as well as in other neuropsychatric disor
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Noha Abdel Halim Mohamed Rezk, "Association of angiotensin II type I and type II receptor genes polymorphisms with the presence of premature coronary disease and metabolic syndrome", springer, 2014
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