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Clinical and Molecular Heterogeneity in Patients with the CblD Inborn Error of Cobalamin Metabolism

✍ Scribed by Isabelle R. Miousse; David Watkins; David Coelho; Tony Rupar; Eric A. Crombez; Eric Vilain; Jonathan A. Bernstein; Tina Cowan; Christopher Lee-Messer; Gregory M. Enns; Brian Fowler; David S. Rosenblatt


Book ID
113745018
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
396 KB
Volume
154
Category
Article
ISSN
1097-6833

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The diets of 5 patients with phenylketonuria or maple-syrup-urine disease were supplemented with yeast which was rich in selenium. For 120 days the patients received 45 gg Se/day to increase the Se content of their diets to 10-12ng Se/Kjoule. Before supplementation the selenium content of serum (5-1