Author:
Rossanti Rini,Nozu Kandai,Fukunaga Atsushi,Nagano China,Horinouchi Tomoko,Yamamura Tomohiko,Sakakibara Nana,Minamikawa Shogo,Ishiko Shinya,Aoto Yuya,Okada Eri,Ninchoji Takeshi,Kato Noritoshi,Maruyama Shoichi,Kono Keiji,Nishi Shinichi,Iijima Kazumoto,Fujii Hideki
Funder
Ministry of Education, Culture, Sports, Science and Technology
Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Nephrology,Physiology
Reference33 articles.
1. Mehta A, et al. Fabry disease: a review of current management strategies. QJM. 2010;103(9):641–59.
2. Desnick RJ. Fabry disease, an under-recognized multisystemic disorder:expert recommendations for diagnosis, management, and enzyme replacement therapy. Ann Intern Med. 2003;138:338–46.
3. Saito S, Ohno K, Sakuraba H. Fabry-database.org: database of the clinical phenotypes genotypes and mutant ⍺-galactosidase A sturctures in Fabry disease. J Hum Genet. 2011;56(6):467–8.
4. Fuller M, Meikle P, Hopwood J. Epidemiology of lysosomal storage diseases: an overview, in Fabry Disease: perspectives from 5 Years of FOS. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Pharmagenesis. England: Oxford; 2006.
5. Sawada T, et al. Newborn screening for Fabry disease in the western region of Japan. Mol Genet Metab Rep. 2020;22:100562.
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