In vitro generated Rh(null) red cells recapitulate the in vivo deficiency: a model for rare blood group phenotypes and erythroid membrane disorders.
Cambot M, Mazurier C, Canoui-Poitrine F, Hebert N, Picot J, Clay D, Picard V, Ripoche P, Douay L, Dubart-Kupperschmitt A, Cartron JP.
Am J Hematol. 2013 May;88(5):343-9. doi: 10.1002/ajh.23414. Epub 2013 Mar 15.
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Extensive clinical, serologic and molecular studies lead to the first reported Rhmod phenotype in Argentina.
Mufarrege N, Franco N, Trucco Boggione C, Arnoni C, de Paula Vendrame T, Bartoli S, Ensinck A, Principi C, Lujan Brajovich M, Mattaloni S, Riquelme B, Biondi C, Castilho L, Cotorruelo C.
Transfusion. 2020 Jul;60(7):1373-1377. doi: 10.1111/trf.15792. Epub 2020 May 6.