View in EDS HTML Full Text PDF Full Text

Rhnull phenotype in an Indian patient due to a novel c.1138 + 2 t > a mutation in the RHAG gene.

Saved in:
Bibliographic Details
Title: Rhnull phenotype in an Indian patient due to a novel c.1138 + 2 t > a mutation in the RHAG gene.
Authors: Banerjee, Soumee1 (AUTHOR) soumee@bmstindia.org, Mathur, Ankit1 (AUTHOR), Hurkat, Neha2 (AUTHOR), Chakraborty, Santanu1 (AUTHOR), Reddy, T. V.1 (AUTHOR)
Source: Transfusion Medicine. Jun2024, Vol. 34 Issue 3, p223-226. 4p.
Database: Academic Search Ultimate
Full text is not displayed to guests.
Description
ISSN:09587578
DOI:10.1111/tme.13045