Zuzana Striezencova Laluhova

Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios

V. Divoky, D. Pospíšilová, K. Indrák, 2014, British journal of haematology.

Molecular characterization of six new cases of red blood cell hexokinase deficiency yields four novel mutations in HK1.

J. Vives Corrons, R. van Wijk, B. V. van Oirschot, 2016, Blood cells, molecules & diseases.

Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios

D. Pospíšilová, K. Indrák, J. Čermák, 2014, British journal of haematology.