CONGENITAL DEFICIENCY OF HUMAN R-TYPE BINDING-PROTEINS OF COBALAMIN
- 1 January 1977
- journal article
- research article
- Vol. 29 (6) , 619-626
Abstract
A family expressing the congenital absence of the R-type binders of cobalamin (Cbl), vitamin B-12, was restudied. The capacity to bind Cbl to R type binders was absent from serum, saliva, cerebrospinal fluid, gastric juice granulocytes, and granulocyte output of the propositus. Serum R did not carry Cbl in vivo. There was no immunological R binder in this saliva, but cross reacting material was detected in his serum. Evidence of a partial expression of the defect was observed in offspring of 2 affected persons. There were no obvious clinical consequences of the defect.This publication has 18 references indexed in Scilit:
- The Failure of Granulocytes to Produce Transcobalamin I (TC I)Scandinavian Journal of Haematology, 2009
- THE PLASMA TRANSPORT OF VITAMIN B12British Journal of Haematology, 1976
- Transcobalamins I and II as natural transport proteins of vitamin B12.Journal of Clinical Investigation, 1975
- Colony Formation by Human Haemopoietic Precursor Cells Cultured in Semi-solid Agar in Diffusion ChambersBritish Journal of Haematology, 1975
- Measurement of vitamin B12-binding proteins of plasma. II. Interpretation of patterns in disease.1975
- Human vitamin B12 transport proteins.1975
- Editorial: Congenital disorders of vitamin B12 transport and their contribution to concepts.1973
- The Content of Vitamin B12 in Adult and Foetal Tissue: A Comparative StudyBritish Journal of Haematology, 1970
- Immunological properties of human vitamin B12 bindersBiochimica et Biophysica Acta (BBA) - Protein Structure, 1970
- Deficiency of Vitamin B12-Binding Alpha Globulin in Two BrothersBlood, 1969