Associated Papers
Severe hypertension caused by 17α-hydroxylase deficiency: A case report.
Zhao Y et al.
Heliyon, 2023
36967917 (PubMed )
Supplement: mmc1.docx
Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation.
Jamwal M et al.
Journal of Clinical Pathology, 2018
A family study of the Chinese Rhnull individual of the regulator type: a novel single missense mutation identified in RHAG gene.
Tian L et al.
Transfusion, 2011
The Rh protein family: gene evolution, membrane biology, and disease association.
Huang CH et al.
Cellular and Molecular Life Sciences : Cmls, 2010
A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein.
Tilley L et al.
Vox Sanguinis, 2010
Molecular biology and genetics of the Rh blood group system.
Huang CH et al.
Seminars in Hematology, 2000
Molecular basis for Rh(null) syndrome: identification of three new missense mutations in the Rh50 glycoprotein gene.
Huang CH et al.
American Journal of Hematology, 1999
Blood group immunochemistry and genetics.
Unknown Author
Seminars in Hematology, 1981
Hydrophobic cluster analysis and modeling of the human Rh protein three-dimensional structures.
Callebaut I et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 0
Select a paper to view details