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Characterizing renal involvement in Hermansky-Pudlak Syndrome in a zebrafish model
Hermansky-Pudlak Syndrome (HPS) is a rare disease caused by mutations in the genes coding for various HPS proteins. HPS proteins are part of multi-subunit complexes involved in the biogenesis of organelles from the lysosomal-endosomal-system. In humans, this syndrome is characterized by the presence...
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| Publicado no: | Sci Rep |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6881439/ https://ncbi.nlm.nih.gov/pubmed/31776394 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-54058-5 |
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