Rhmod Syndrome: A Family Study of the Translation-Initiator Mutation in the Rh50 Glycoprotein Gene
- 1 January 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (1), 108-117
- https://doi.org/10.1086/302215
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- A splicing mutation of the RHAG gene associated with the Rhnull phenotypeAnnals of Human Genetics, 1998
- Identification of 5′ Flanking Sequence ofRH50Gene and the Core Region for Erythroid-Specific ExpressionBiochemical and Biophysical Research Communications, 1998
- The Human Rh50 Glycoprotein GeneJournal of Biological Chemistry, 1998
- A human monoclonal anti‐D antibody which detects a nonconformation‐dependent epitope on the RhD protein by immunoblotBritish Journal of Haematology, 1997
- The β- and δ-Thalassemia Repository (Eighth Edition)Hemoglobin, 1995
- Murine monoclonal antibody MB‐2D10 recognizes Rh‐related glycoproteins in the human red cell membraneTransfusion, 1990
- Regulator Genes Affecting Red Cell AntigensTransfusion Medicine Reviews, 1990
- Hematological aspect of Rh deficiency syndrome: A case report and a review of the literatureAmerican Journal of Hematology, 1987
- Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proceedings of the National Academy of Sciences, 1979
- Rhmod, a Second Kindred (Craig)1Vox Sanguinis, 1976