Inheritance of transcobalamin II (TC II) in two families with TC II deficiency and related immunodeficiency
- 1 December 1981
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 4 (1), 165-166
- https://doi.org/10.1007/bf02263642
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Abnormal biochemistry and morphology of erythrocytes in a case of transcobalamin II deficiency during treatmentJournal of Inherited Metabolic Disease, 1981
- Polymorphic variants of transcobalamin II rare alleles in family studiesPublished by Walter de Gruyter GmbH ,1979
- Radioimmunosorbent determinations of unsaturated and total transcobalamin II in human serumPublished by Walter de Gruyter GmbH ,1979
- Inherited Lack of Transcobalamin II in Serum and Megaloblastic Anaemia: a Further PatientBritish Journal of Haematology, 1979
- Studies on transcobalamin (TC). 1. Detection of TC II isoproteins in human serumBlood, 1979
- Transport of therapeutic cyanocobalamin in the congenital deficiency of transcobalamin II (TC II)Blood, 1979
- Hereditary transcobalamin II deficiency: Clinical findings in a new familyThe Journal of Pediatrics, 1974
- Hereditary transcobalamin II deficiency: The role of transcobalamin II in vitamin B12-mediated reactionsThe Journal of Pediatrics, 1972