PKU, Sorbitol, & Galactose/Fructose Disorders
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Phenylketonuria (PKU) Phenylketonuria (PKU) is a genetic deficiency of either Phenylalanine Hydroxylase or its cofactor, Tetrahydrobiopterin (THB). This inhibits the conversion of Phenylalanine to …
PKU, Sorbitol, Galactose & Fructose. Flashcards
PKU, Phenylketonuria, Galactosemia, Hereditary Fructose Intolerance & Sorbitol Diabetic Cataracts
USMLE Step 1- Lesson 60 - Fructose and Galactose metabolism and deficiencies
Hereditary Fructose Intolerance - ScienceDirect
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PKU, Phenylketonuria, Galactosemia, Hereditary Fructose Intolerance & Sorbitol Diabetic Cataracts
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IJMS, Free Full-Text
Sweet and sour: an update on classic galactosemia - Coelho - 2017 - Journal of Inherited Metabolic Disease - Wiley Online Library
