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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Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: Ballesteros Reviriego, Carmen, Clare, Simon, Arends, Mark J., Cambridge, Emma L., Swiatkowska, Agnieszka, Caetano, Susana, Abu-Helil, Bushra, Kane, Leanne, Harcourt, Katherine, Goulding, David A., Gleeson, Diane, Ryder, Edward, Doe, Brendan, White, Jacqueline K., van der Weyden, Louise, Dougan, Gordon, Adams, David J., Speak, Anneliese O.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2019
Konular:
Research Article
Online Erişim: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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