Článek v časopise Publikováno 2017

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

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)

Zobrazit v PubMed Citovat

2017 Rok
28803808 PMID

Citace publikace

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.

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

Citace publikace

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