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Hypertrophic cardiomyopathy in late-onset variant of Fabry disease with high residual activity of α-galactosidase A

✍ Scribed by Yoshiro Nagao; Haruko Nakashima; Yukiko Fukuhara; Michie Shimmoto; Akihiro Oshima; Yuji Ikari; Yoshio Mori; Hitoshi Sakuraba; Yoshiyuki Suzuki


Book ID
115090174
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
310 KB
Volume
39
Category
Article
ISSN
0009-9163

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Residual activity of α-galactosidase A i
✍ Giovanni Romeo; Michele D'Urso; Alfredo Pisacane; Eric Blum; Antonio Falco; Anna 📂 Article 📅 1975 🏛 Springer 🌐 English ⚖ 602 KB

The alpha-galactosidase A activity from fibroblasts of five Fabry patients and five controls has been separated from alpha-galactosidase B through small DEAE-cellulose columns and in some experiments by treatment of the fibroblast extracts with Sepharose coupled to anti-alpha-galactosidase B antibod