Associated Papers
A stepwise diagnostic approach for undiagnosed Anemia in children: A model for low-middle income country.
Aly NH et al.
Blood Cells, Molecules & Diseases, 2023
[Identification and characterization of PKLR gene mutation in two patients with erythrocyte pyruvate kinase deficiency].
Huang ZD et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2017
Multi-omics of 34 colorectal cancer cell lines - a resource for biomedical studies.
Berg KCG et al.
Molecular Cancer, 2017
28683746 (PubMed )
Supplement: 12943_2017_691_MOESM1_ESM.xlsx › Table_S5
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.
Mojzikova R et al.
British Journal of Haematology, 2014
Six previously undescribed pyruvate kinase mutations causing enzyme deficiency.
Demina A et al.
Blood, 1998
Pyruvate kinase deficient hemolytic anemia in the Northern Irish population.
Percy MJ et al.
Blood Cells, Molecules & Diseases, 0
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