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Molecular architecture of the Bardet–Biedl syndrome protein 2-7-9 subcomplex
Bardet-Biedl syndrome (BBS) is a genetic disorder characterized by malfunctions in primary cilia resulting from mutations that disrupt the function of the BBSome, an 8-subunit complex that plays an important role in protein transport in primary cilia. To better understand the molecular basis of BBS,...
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| Publicado no: | J Biol Chem |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Biochemistry and Molecular Biology
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6827290/ https://ncbi.nlm.nih.gov/pubmed/31530639 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA119.010150 |
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