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Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chainl-3-hydroxyacyl-CoA dehydrogenase deficiency

✍ Scribed by J. Bergoffen; P. Kaplan; D. E. Hale; M. J. Bennett; G. T. Berry


Publisher
Springer
Year
1993
Tongue
English
Weight
342 KB
Volume
16
Category
Article
ISSN
0141-8955

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