Gilbert’s syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II)
- 1 April 2000
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 136 (4) , 556-559
- https://doi.org/10.1016/s0022-3476(00)90026-x
Abstract
No abstract availableKeywords
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- Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemiaProceedings of the National Academy of Sciences, 1997
- The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulumBlood, 1996
- The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's SyndromeNew England Journal of Medicine, 1995
- Pigment Gallstone DiseaseGastroenterology Clinics of North America, 1991