Fabry disease: Mechanism and therapeutics strategies
Fabry disease is a monogenic disease characterized by a deficiency or loss of the α-galactosidase A (GLA). The resulting impairment in lysosomal GLA enzymatic activity leads to the pathogenic accumulation of enzymatic substrate and, consequently, the progressive appearance of clinical symptoms in ta...
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| Автори: | , , , , , |
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| Формат: | Книга |
| Опубліковано: |
Frontiers Media S.A.,
2022-10-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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| Примірник 1 | Доступно |