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Gaucher Disease: Progress and Ongoing Challenges
Over the past decades, tremendous progress has been made in the field of Gaucher disease, the inherited deficiency of the lysosomal enzyme glucocerebrosidase. Many of the colossal achievements took place during the course of the sixty-year tenure of Dr. Roscoe Brady at the National Institutes of Hea...
Tallennettuna:
| Julkaisussa: | Mol Genet Metab |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5425955/ https://ncbi.nlm.nih.gov/pubmed/27916601 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2016.11.006 |
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