TY  - GEN
AU  - Brivet,M
AU  - Moatti,N
AU  - Corriat,A
AU  - Lemonnier,A
AU  - Odievre,M
TI  - Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome
SN  - 0031-3998
PY  - 1983///0415
KW  - Child, Preschool
KW  - Erythrocytes
KW  - metabolism
KW  - Fanconi Syndrome
KW  - complications
KW  - Female
KW  - Galactose
KW  - Glucagon
KW  - Glucose
KW  - Glycogen Storage Disease
KW  - Glycolysis
KW  - Humans
KW  - In Vitro Techniques
KW  - Kidney
KW  - Liver
KW  - Liver Function Tests
KW  - Oxidation-Reduction
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1203/00006450-198302000-00015
ER  -