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Structural Mapping of Missense Mutations in the Pex1/Pex6 Complex
Peroxisome biogenesis disorders (PBDs) are nontreatable hereditary diseases with a broad range of severity. Approximately 65% of patients are affected by mutations in the peroxins Pex1 and Pex6. The proteins form the heteromeric Pex1/Pex6 complex, which is important for protein import into peroxisom...
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| Pubblicato in: | Int J Mol Sci |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6696164/ https://ncbi.nlm.nih.gov/pubmed/31374812 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20153756 |
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