Original Articles and Brief Reports

The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W)

Division of Neonatology, University Hospital Merkur, Zagreb, Croatia
Division of Hematology, University of Utah, Salt Lake City, UT, USA;Department of Biology, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic
Department of Human Genetics, University of Utah, Salt Lake City, UT, USA
Department of Pediatrics, Division of Hematology, University Hospital Center, Zagreb, Croatia
Division of Hematology, University of Utah, Salt Lake City, UT, USA
Chuvash Republic Clinical Hospital No. 1, Cheboksary, Russia
Cheboksary Children's Hospital, Cheboksary, Russia
Center for Sickle Cell Disease and Department of Medicine, Howard University, Washington, DC, USA
Center for Sickle Cell Disease and Department of Medicine, Howard University, Washington, DC, USA
Sickle Cell Center and Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA
Division of Hematology, University of Utah, Salt Lake City, UT, USA
Vol. 98 No. 4 (2013): April, 2013 https://doi.org/10.3324/haematol.2012.070508