Enzyme replacement therapy in heterozygous females with Fabry disease: Results of a phase IIIB study
Author:
Affiliation:
1. ; Children's Hospital; Johannes-Gutenberg University; Mainz Germany
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/B:BOLI.0000005658.14563.77/fullpdf
Reference25 articles.
1. Enzymatic defect in Fabry's disease;Brady;N Engl J Med,1967
2. Value of echocardiographic measurement of left ventricular mass in predicting cardiovascular morbid events in hypertensive men;Casale;Ann Intern Med,1986
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