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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant

Fig. 2

a Distribution of residual GLA activities in patients with p.A143T and Fabry disease patients with other missense GLA mutations. b Correlation of residual GLA activities with lyso-Gb3 levels in male Fabry disease patients with other missense GLA mutations and c in male patients with p.A143T. The dotted line represents the upper reference value of measured lyso-Gb3 (0.9 ng/ml). Values are given as medians with 5–95 % confidence intervals

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