A novel A97P amino acid substitution in α‐galactosidase A leads to a classical Fabry disease with cardiac manifestations
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Y. Onodera | K. Kimura | H. Nakamura | K. Sato-Matsumura | T. Takahashi | K. Morita | N. Enami | T. Shougase | T. Ohsaki | M. Kato | Y. Yamaguchi | H. Shimizu