Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision

Overview of attention for article published in Journal of Inherited Metabolic Disease, November 2016

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Glutaric aciduria type 1

Cited by user Chris Capoccia on 02 Jul 2020

Glutaric acidemia type 1 is an inherited disorder in which the body is unable to completely break down the amino acids lysine, hydroxylysine and tryptophan.