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Fig. 4 | Cellular & Molecular Biology Letters

Fig. 4

From: A rare mutation (p.F149del) of the NT5C3A gene is associated with pyrimidine 5′-nucleotidase deficiency

Fig. 4

Significant decline in enzymatic activity in HA patients’ (RK and MK) erythrocytes hemolysate caused by lack of cytosolic pyrimidine 5′-nucleotidase. The results for RK and MK are statistically significant at p < 0.001 in relation to asymptomatic family members (EK, AK) (for all family members we used technical replicates) and the control group (for four healthy individuals we used biological and technical replicates). Student’s t-test, ***p < 0.001. Error bars represent standard deviation

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Cellular & Molecular Biology Letters

ISSN: 1689-1392

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