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pro vyhledávání: '"徐明嘉"'
Autor:
Ming-Jia Hsu, 徐明嘉
105
Fabry disease (FD) is a hereditary disease defined by mutations of alpha-galactosidase A (GLA), a lysosomal enzyme responsible for breaking down glycosphingolipids (GSL). Defective GLA activity leads to the accumulation of globotriaosylceram
Fabry disease (FD) is a hereditary disease defined by mutations of alpha-galactosidase A (GLA), a lysosomal enzyme responsible for breaking down glycosphingolipids (GSL). Defective GLA activity leads to the accumulation of globotriaosylceram
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/jjsjb5
