A carboxy-terminal truncation of human alpha-galactosidase A in a heterozygous female with Fabry disease and modification of the enzymatic activity by the carboxy-terminal domain. Increased, reduced, or absent enzyme activity depending on number of amino acid residues deleted.

Source:http://linkedlifedata.com/resource/pubmed/id/8878432

J. Clin. Invest. 1996 Oct 15 98 8 1809-17

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PMID
8878432