Author:
Bouwman Machtelt G.,Rombach Saskia M.,Schenk Erica,Sweeb Annelies,Wijburg Frits A.,Hollak Carla E. M.,Linthorst Gabor E.
Subject
Genetics (clinical),Genetics
Reference24 articles.
1. Bland JM, Altman DG (1995) Multiple significance tests: the Bonferroni method. BMJ 310(6973):170
2. Bouwman MG, Hollak CE, van den Bergh Weerman MA, Wijburg FA, Linthorst GE (2010) Analysis of placental tissue in Fabry disease with and without enzyme replacement therapy. Placenta 31(4):344–346
3. Deegan PB, Baehner AF, Barba Romero MA, Hughes DA, Kampmann C, Beck M (2006) Natural history of Fabry disease in females in the Fabry outcome survey. J Med Genet 43(4):347–352
4. Desnick RJ, Ioannou YA, Eng CM (2001) A-galactosidase A deficiency: Fabry disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease, 8th edn. McGraw-Hill, NewYork, pp 3733–3774
5. Galanos J, Nicholls K, Grigg L, Kiers L, Crawford A, Becker G (2002) Clinical features of Fabry's disease in Australian patients. Intern Med J 32(12):575–584
Cited by
26 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献