Perinatal Diagnosis of Type 1c Glycogen Storage Disease
- 1 April 1989
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 12 (S2) , 315-317
- https://doi.org/10.1007/bf03335409
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- A new microtechnique for the analysis of the human hepatic microsomal glucose-6-phosphatase systemClinica Chimica Acta; International Journal of Clinical Chemistry, 1988
- The identification of T2; the phosphate/pyrophosphate transport protein of the hepatic microsomal glucose‐6‐phosphatase systemFEBS Letters, 1988
- The phosphohydrolase component of the hepatic microsomal glucose-6-phosphatase system is a 36.5-kilodalton polypeptide.Journal of Biological Chemistry, 1988
- The mechanism of histone activation of the hepatic microsomal glucose-6-phosphatase system: a novel method to assay glucose-6-phosphatase activityBiochimica et Biophysica Acta (BBA) - General Subjects, 1988
- DIAGNOSIS OF TYPE 1a AND TYPE 1c GLYCOGEN STORAGE DISEASES IN ADULTSThe Lancet, 1987