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Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers
- Correspondence to: Professor E Zammarchi, Metabolic and Neuromuscular Unit, Department of Paediatrics, University of Florence, Meyer Children’s Hospital, Via L Giordano 13, Florence, Italy; malmetab{at}unifi.it
Citation
Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers
Publication history
- First published August 14, 2003.
Online issue publication
April 27, 2016
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Copyright 2003 Journal of Medical Genetics