Heterozygosity for bisphosphoglycerate mutase deficiency expressing clinically as congenital erythrocytosis: A case series and literature review

por van Dijk, Myrthe J., van Oirschot, Brigitte A., Stam‐Slob, Manon C., Waanders, Esmé, van der Zwaag, Bert, van Beers, Eduard J., Jans, Judith J. M., van der Linden, Peter Willem, Torregrosa Diaz, Jose M., Gardie, Betty, Girodon, François, Schots, Rik, Thielen, Noortje, van Wijk, Richard
Publicado 2022