3-Hydroxy-3-methylglutaryl-CoA lyase deficiency.

Authors :: Walter JH
Clayton PT
Leonard JV
Source :: Journal of inherited metabolic disease [J Inherit Metab Dis] 1986; Vol. 9 (3), pp. 287-8.
Publication Year :: 1986

Subjects :: Amino Acid Metabolism, Inborn Errors genetics
Ammonia blood
Female
Genetic Carrier Screening
Humans
Hypoglycemia enzymology
Infant
Amino Acid Metabolism, Inborn Errors enzymology
Oxo-Acid-Lyases deficiency
Reye Syndrome enzymology

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