MGA

(redirected from 3-Methylglutaconic aciduria)
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AcronymDefinition
MGAMorris Garage Type A (English sports car )
MGAMicro Games of America
MGAMultiobjective Genetic Algorithm (computer science)
MGAMicrosoft Genuine Advantage (anti-piracy system)
MGAMalagasy Ariary (ISO currency code)
MGAMember and Geographic Activities (IEEE)
MGAManagua, Nicaragua (Airport Code)
MGAMedley Global Advisors (New York)
MGAMyasthenia Gravis Association (UK)
MGAMidwestern Governors Association (Washington, DC)
MGAManaging General Agent (insurance)
MGAMasters in Government Administration (degree program; University of Pennsylvania)
MGAMultimode Graphics Adapter
MGAMeteorological and Geophysical Agency (Indonesia)
MGAMetal Gear Acid (gaming)
MGAMelengestrol Acetate (synthetic progesterone)
MGAMessy Genetic Algorithm (heredity)
MGAMonochrome Graphics Adapter
MGAManagement Général Avancé (French: Advanced General Management)
MGA3-Methylglutaconic Aciduria
MGAMiddle Gimbal Angle (astronomy)
MGAMalaysian Golf Association
MGAMailorder Gardening Association
MGAMedium Gain Antenna
MGAMichigan Guaranty Agency (Michigan Higher Education Assistance Authority)
MGAMegaloblastic Anemia
MGAMajor Graded Area
MGAMatrox Graphics Adapter
MGAMicro-Genetic Algorithm
MGAMacdougall Gabriel Associates (UK)
MGAMathew Greenwald Associates (market research: Washington, DC)
MGAManitoba Golf Association (Canada)
MGAMultiple Gas Analyzer
MGAMutuelle Générale d'Assurances (French: General Mutual Insurance)
MGAMicro Gas Analyzer
MGAMultiple Group Analysis
MGAMaster Graphoanalyst
MGAManitoba Go Association
MGAManitoba Goat Association (Manitoba, Canada)
MGAMaster Government Appraiser
MGAMichigan Gazehound Association
MGAMature Gaming Association (gaming guild)
MGAMaster General Agents/Brokers (financial)
MGAMichigan Gamers Association (University of Michigan)
MGAMessage Guidance Area
MGAMonterey Green Action
References in periodicals archive ?
Human Disorders: OPA3 Mutations Causing ADOA and Cataract (ADOAC) and Type III 3-Methylglutaconic Aciduria
Type III 3-methylglutaconic aciduria (OMIM 25801, also known as Costeff syndrome) is a rare neuroophthalmological syndrome characterized by increased urinary excretion of 3-methylglutaconic acid and 3-methylglutaric acid, early-onset bilateral optic atrophy, pallor of the optic disk, and reduced visual acuity, which are associated with spasticity, extrapyramidal signs, and cognitive deficits in later stages of the disease.
Elpeleg, "Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews," American Journal of Human Genetics, vol.
Ly et al., "OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondria," Molecular Genetics and Metabolism, vol.
Inherited 3-methylglutaconic aciduria in two brothers-another defect of leucine metabolism.
3-Methylglutaconic aciduria type I: clinical heterogeneity as a neurometabolic disease.
Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria. J Pediatr 1991;118:885-90.
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