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Fabry disease: Characterization of α-galactosidase A double mutations and the D313Y plasma enzyme pseudodeficiency allele
Makiko Yasuda, Junaid Shabbeer, Stacy D. Benson, Irene Maire, Roger M. Burnett, Robert J. DesnickVolume:
22
Année:
2003
Langue:
english
Pages:
7
DOI:
10.1002/humu.10275
Fichier:
PDF, 372 KB
english, 2003