Molecular Investigation of Glutaric Aciduria Type1 in Iran

Glutaric Acidemia, Type I (GA I), was first described in 1975. The disease is caused by a genetic deficiency of the enzyme, Glutaryl-CoA Dehydrogenase (GCD), which leads to the buildup of Glutaric acid in the tissues and its excretion in the urine of affected patients. GCD is involved in the catabol...

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Bibliographic Details
Main Authors: HOUSHMAND, Massoud, ARYANI, Omid, PIRZADEH, Zahra, GHASEMI, Fereshteh, SALEHPOUR, Shadab, TEHRANI, Freshteh
Format: Online
Language:eng
Published: Iranian Journal of Child Neurology 2012
Online Access:http://journals.sbmu.ac.ir/ijcn/article/view/2905

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