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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Detalles Bibliográficos
Autores principales: Schenk, H., Müller-Deile, J., Schroder, P., Bolaños-Palmieri, P., Beverly-Staggs, L., White, R., Bräsen, J. H., Haller, H., Schiffer, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881439/
https://www.ncbi.nlm.nih.gov/pubmed/31776394
http://dx.doi.org/10.1038/s41598-019-54058-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881439/
https://www.ncbi.nlm.nih.gov/pubmed/31776394
http://dx.doi.org/10.1038/s41598-019-54058-5

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