The detection of molybdenum cofactor deficiency: clinical symptomatology and urinary metabolite profile.

Authors :: van Gennip AH
Abeling NG
Stroomer AE
Overmars H
Bakker HD
Source :: Journal of inherited metabolic disease [J Inherit Metab Dis] 1994; Vol. 17 (1), pp. 142-5.
Publication Year :: 1994

Subjects :: Amino Acids urine
Child, Preschool
Chromatography, High Pressure Liquid
Humans
Infant, Newborn
Molybdenum Cofactors
Purines urine
Sulfates urine
Coenzymes
Metal Metabolism, Inborn Errors urine
Metalloproteins metabolism
Pteridines metabolism

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