Type IV glycogen storage disease: Branching enzyme deficiency in skin fibroblasts and possible heterozygote detection
- 30 April 1971
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 78 (4) , 638-642
- https://doi.org/10.1016/s0022-3476(71)80466-3
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Simultaneous absence of α-1,4-glucosidase and α-1,6-glucosidase activities (pH 4) in tissues of children with Type II glycogen storage diseaseBiochemistry, 1970
- Studies on leukocyte brancher enzyme activityin a family with type IV glycogenosisThe Journal of Pediatrics, 1969
- Glycogen storage disease type IV, amylopectinosis.Archives of Disease in Childhood, 1968
- Branching enzyme-deficiency glycogenosis: studies in therapy.Archives of Disease in Childhood, 1968
- Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis.Proceedings of the National Academy of Sciences, 1966
- Structure of Glycogens and AmylopectinsPublished by Elsevier ,1952