Differential assay for lysosomal alpha-galactosidases in human tissues and its application to Fabry's disease

Author:

Mayes Jary S.,Scheerer Julia B.,Sifers Richard N.,Donaldson Mark L.

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference19 articles.

1. Variability of α-galactosidase A and B in different tissues of man;Beutler;Am. J. Hum. Genet.,1973

2. Fabry's disease: Structural or regulatory mutation?;Beutler;J. Lab. Clin. Med.,1971

3. On the existence and the enzymatic interconversion of the isozymes of α-galactosidase in human organs;Kint;Arch. Int. Physiol. Biochem.,1971

4. Purification and properties of the two major isozymes of α-galactosidase from human placenta;Kusiak;J. Biol. Chem.,1978

5. The identification of α-galactosidase B from human liver as an α -N-acetylgalactosaminidase;Dean;Biochem. Biophys. Res. Commun.,1977

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