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FBXO7 sensitivity of phenotypic traits elucidated by a hypomorphic allele
FBXO7 encodes an F box containing protein that interacts with multiple partners to facilitate numerous cellular processes and has a canonical role as part of an SCF E3 ubiquitin ligase complex. Mutation of FBXO7 is responsible for an early onset Parkinsonian pyramidal syndrome and genome-wide associ...
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| Publicado no: | PLoS One |
|---|---|
| Main Authors: | , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6402633/ https://ncbi.nlm.nih.gov/pubmed/30840666 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0212481 |
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