Fabry disease: 45 novel mutations in the α-galactosidase A gene causing the classical phenotype

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Academic Press

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Blood group does not correlate with disease severity in patients with Fabry disease ( -galactosidase A deficiency)

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Elsevier

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Splenomegaly, hypersplenism and peripheral blood cytopaenias in patients with classical Anderson-Fabry disease

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Springer Publishing Company

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Fibroblast Activation Protein in Remodeling Tissues

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Current Molecular Medicine, Vol. 12, Iss. 10, 2012-12 ,pp. : 1220-1243

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