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pro vyhledávání: '"Yuya Tayama"'
Autor:
Takahiro Tsukimura, Yuya Tayama, Tomoko Shiga, Kanako Hirai, Tadayasu Togawa, Hitoshi Sakuraba
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100650- (2020)
Enzyme replacement therapy (ERT) for Fabry disease (deficiency of α-galactosidase A, α-Gal) with recombinant α-Gals (agalsidase alfa and agalsidase beta) is widely available and improves some of the clinical manifestations and biochemical findings
Externí odkaz:
https://doaj.org/article/b92eff7f1b5d48e2800f21ec83adfb7f
Autor:
Hitoshi Sakuraba, Tomoko Shiga, Takahiro Tsukimura, Kanako Hirai, Yuya Tayama, Tadayasu Togawa
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100650-(2020)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Enzyme replacement therapy (ERT) for Fabry disease (deficiency of α-galactosidase A, α-Gal) with recombinant α-Gals (agalsidase alfa and agalsidase beta) is widely available and improves some of the clinical manifestations and biochemical findings
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a05bb52d893fdec34ea9260598e60c1c
https://doi.org/10.1016/j.ymgmr.2020.100650
https://doi.org/10.1016/j.ymgmr.2020.100650