Standardization of nomenclature for transcobalamin II variants
- 1 September 1982
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 61 (2), 165-166
- https://doi.org/10.1007/bf00274211
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Inheritance of transcobalamin II (TC II) in two families with TC II deficiency and related immunodeficiencyJournal of Inherited Metabolic Disease, 1981
- Studies of a Patient with Megaloblastic Anemia and an Abnormal Transcobalamin IINew England Journal of Medicine, 1980
- Report of nomenclature meeting for α1-antitrypsinHuman Genetics, 1980
- [Transcobalamine-II-polymorphism: biochemical and clinical aspects of rare variants].1979
- Inherited Lack of Transcobalamin II in Serum and Megaloblastic Anaemia: a Further PatientBritish Journal of Haematology, 1979
- International System for Human Gene Nomenclature (1979) ISGN (1979)Cytogenetic and Genome Research, 1979
- STUDIES ON TRANSCOBALAMIN (TC) .1. DETECTION OF TC-II ISOPROTEINS IN HUMAN-SERUM1979
- Detection of genetic variation with radioactive ligands. III. genetic polymorphism of transcobalamin II in human plasma.1978
- Hereditary transcobalamin II deficiency: Clinical findings in a new familyThe Journal of Pediatrics, 1974
- Neonatal Megaloblastic Anemia Due to Inherited Transcobalamin II Deficiency in Two SiblingsNew England Journal of Medicine, 1971