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    Zampetti, A., Fania, L., Antuzzi, D., Giurdanella, F., Gnarra, M., Bertola, F., Lualdi, S., Filocamo, M., Morrone, A., & Feliciani, C. (n.d.). mutation identification of Fabry disease in families with other lysosomal storage disorders. Clinical genetics, 84, 281–285. http://access.bl.uk/ark:/81055/vdc_100043490052.0x000001
  
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