Molecular characterization of six new cases of red blood cell hexokinase deficiency yields four novel mutations in HK1
Koralkova, Pavla, Mojzikova, Renata, van Oirschot, Brigitte, Macartney, Christine, Timr, Pavel, Vives Corrons, Joan Lluis, Striezencova Laluhova, Zuzana, Lejhancova, Katerina, Divoky, Vladimir, van WiVolume:
59
Language:
english
Journal:
Blood Cells, Molecules, and Diseases
DOI:
10.1016/j.bcmd.2016.04.002
Date:
July, 2016
File:
PDF, 919 KB
english, 2016