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Carboxyl-Terminal Truncations Alter the Activity of the Human α-Galactosidase A
Fabry disease is an X-linked inborn error of glycolipid metabolism caused by deficiency of the human lysosomal enzyme, α-galactosidase A (αGal), leading to strokes, myocardial infarctions, and terminal renal failure, often leading to death in the fourth or fifth decade of life. The enzyme is respons...
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| Publicado no: | PLoS One |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4342250/ https://ncbi.nlm.nih.gov/pubmed/25719393 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0118341 |
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