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Anderson-Fabry disease in heart failure
Anderson-Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the GLA gene that result in deficiency of the enzyme alpha-galactosidase A. The worldwide incidence of Fabry’s disease is reported to be in the range of 1 in 40,000–117,000, although this value may be a significa...
Enregistré dans:
| Publié dans: | Biophys Rev |
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| Auteurs principaux: | , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Springer Berlin Heidelberg
2018
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6082315/ https://ncbi.nlm.nih.gov/pubmed/29909504 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12551-018-0432-5 |
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