Skip to main content

Journal article Published 2017

Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin

Authors

R. Mojzikova, Pavla Kořalková, Dušan Holub, Z. Saxova, Dagmar Pospíšilová, D. Prochazkova, Petr Džubák, Monika Horváthová, Vladimír Divoký

Blood cells, molecules & diseases 69, 23-29 (2017)

Cite this publication

MOJZIKOVA, R., P. KOŘALKOVÁ, D. HOLUB, Z. SAXOVA, D. POSPÍŠILOVÁ, D. PROCHAZKOVA, P. DŽUBÁK, M. HORVÁTHOVÁ, V. DIVOKÝ: Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin. Blood cells, molecules & diseases. 2017, 69, 23-29, ISSN: 1079-9796, PMID: 28803808.