Diagnosis of type 1B and 1C glycogen storage disease
- 1 May 1991
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 14 (3) , 305-307
- https://doi.org/10.1007/bf01811688
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- The ontogeny of human hepatic microsomal glucose-6-phosphatase proteinsClinical Chemistry, 1990
- Molecular pathology of glucose‐6‐phosphatase 1The FASEB Journal, 1990
- A new microtechnique for the analysis of the human hepatic microsomal glucose-6-phosphatase systemClinica Chimica Acta; International Journal of Clinical Chemistry, 1988
- DIAGNOSIS OF TYPE 1a AND TYPE 1c GLYCOGEN STORAGE DISEASES IN ADULTSThe Lancet, 1987
- Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system.Journal of Biological Chemistry, 1980
- A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport systemBiochemical and Biophysical Research Communications, 1978