New drugs for the treatment of Anderson–Fabry disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://link.springer.com/content/pdf/10.1007/s40620-020-00721-4.pdf
Reference58 articles.
1. Germain PD (2010) Fabry disease. Orphan J Rare Dis 5:30
2. Arends M, Wanner C, Hughes D et al (2017) Characterization of classical and non-classical Fabry disease. J Am Soc Nephrol 28:1631–1641
3. Echevarria L, Benistan K, Toussaint A et al (2016) X-chromosome inactivation in female patients with Fabry disease. Clin Genet 89(1):44–54
4. Linthorst GE, Bouwman MG, Wijburg FA et al (2010) Screening for Fabry disease in high-risk populations: a systematic review. J Med Genet 47(4):217–222
5. Germain DP, Charrow J, Desnick RJ (2015) Ten-year outcome of enzyme replacement therapy with agalsidase beta in patients with Fabry disease. J Med Genet 52(5):353–358
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