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Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset <i>GLA<\/i> mutation c.936+919G&gt;A (IVS4+919G&gt;A). Hum Mutat 30: 1397-1405, 2009.","DOI":"10.1002\/humu.21074"},{"key":"6","unstructured":"6. Desnick RJ, Ioannou YA, Eng CM. &alpha;-Galactosidase A Deficiency: Fabry Disease. 8th ed. McGraw-Hill, New York, 2001."},{"key":"7","unstructured":"7. Nakao S, Kodama C, Takenaka T, et al. Fabry disease: detection of undiagnosed hemodialysis patients and identification of a \"renal variant\" phenotype. Kidney Int 64: 801-807, 2003."},{"key":"8","unstructured":"8. Wattanasirichaigoon D, Svasti J, Cairns JR, et al. Clinical and molecular characterization of an extended family with Fabry disease. J Med Assoc Thai 89: 1528-1535, 2006."},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. McNair WP, Ku L, Taylor MR, et al. <i>SCN5A<\/i> mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia. 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Acharya D, Robertson P, Neal Kay G, et al. Arrhythmias in Fabry cardiomyopathy. Clin Cardiol 35: 738-740, 2012.","DOI":"10.1002\/clc.22047"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Shah JS, Hughes DA, Sachdev B, et al. Prevalence and clinical significance of cardiac arrhythmia in Anderson-Fabry disease. 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