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Galactose Metabolism in a Patient with Hereditary Galactokinase Deficiency

โœ Scribed by Richard Gitzelmann; Henry J. Wells; Stanton Segal

Book ID
114725561
Publisher
John Wiley and Sons
Year
1974
Tongue
English
Weight
568 KB
Volume
4
Category
Article
ISSN
0014-2972

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๐Ÿ“œ SIMILAR VOLUMES

Galactose and glucose metabolism in gala
Galactose and glucose metabolism in galactokinase deficient, galactose-1-P-uridyl transferase deficient and normal human fibroblasts
โœ Thomas B. Friedman; Rhoda J. Yarkin; Carl R. Merril ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 708 KB

## Abstract Despite the genetic interruption of the Leloir pathway both galactosemic patients and galactosemic fibroblasts can convert galactose to CO~2~ and TCA precipitable products, although at less than the normal rate. These observations stimulated investigations into the identity of the alter