Anderson-Fabry's disease: α galactosidase deficiency
- 13 January 2001
- journal article
- case report
- Published by Elsevier in The Lancet
- Vol. 357 (9250) , 138-140
- https://doi.org/10.1016/s0140-6736(00)03554-6
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Circulating alpha-Galactosidase A Derived from Transduced Bone Marrow Cells: Relevance for Corrective Gene Transfer for Fabry DiseaseHuman Gene Therapy, 1999
- Accelerated transport and maturation of lysosomal α–galactosidase A in Fabry lymphoblasts by an enzyme inhibitorNature Medicine, 1999
- Fabry's disease: a multidisciplinary disorderPublished by Oxford University Press (OUP) ,1997
- An Atypical Variant of Fabry's Disease in Men with Left Ventricular HypertrophyNew England Journal of Medicine, 1995