Article
Rhnull phenotype in an Indian patient due to a novel c.1138 + 2 t > a mutation in the RHAG gene.
Transfusion medicine (Oxford, England) - 1 Jun 2024
Banerjee Soumee, Mathur Ankit, Hurkat Neha, Chakraborty Santanu, Reddy T V
Abstract excerpt
BACKGROUND: The Rh system is an extremely important RBC antigen system with over 50 antigens, 5 of which (D, C, E, c and e) are considered most clinically significant. The rare Rhnull phenotype can result from mutations in the RHD and RHCE genes or the RHAG gene that affects their expression. This is a case report of the second type. CASE REPORT: This case reports a multiparous lady who had to be evaluated for a...
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