Glutaric acidemia type 1 (or "Glutaric Aciduria", "GA1", or "GAT1") is an inherited disorder in which the body is unable to break down completely the amino acids ...
Glutaric acidemia type I is an inherited disorder in which the body is unable to process certain proteins properly. People with this disorder have ...
Introduction. Glutaric aciduria type I (synonym, glutaric acidemia type I) is an autosomal recessive disease caused by inherited deficiency of glutaryl-CoA ...
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What causes glutaric aciduria? Glutaric aciduria is a genetic disorder in which mutations in certain genes cause a deficiency or reduce the efficiency of certain enzymes.
Biochemistry. Glutaric acid is naturally produced in the body during the metabolism of some amino acids, including lysine and tryptophan. Defects in this metabolic ...
Glutaric acidemia type II is an inherited disorder that interferes with the body's ability to break down proteins and fats to produce energy. Incompletely ...
Looking for online definition of glutaricaciduria in the Medical Dictionary? glutaricaciduria explanation free. What is glutaricaciduria?
Disease name: Glutaric acidemia, type 1 Acronym: GA-1. What is GA-1? What causes GA-1? If GA-1 is not treated, what problems occur? What is the treatment for GA-1?
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