The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development

Ciliopathies represent a growing group of human genetic diseases whose etiology lies in defects in ciliogenesis or ciliary function. Given the established entity of renal–retinal ciliopathies, we have been examining the role of cilia-localized proteins mutated in retinitis pigmentosa (RP) in regulat...

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Bibliographische Detailangaben
Hauptverfasser: Hurd, Toby, Zhou, Weibin, Jenkins, Paul, Liu, Chia-Jen, Swaroop, Anand, Khanna, Hemant, Martens, Jeffrey, Hildebrandt, Friedhelm, Margolis, Ben
Format: Artigo
Sprache:Inglês
Veröffentlicht: Oxford University Press 2010
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Articles
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2957320/
https://ncbi.nlm.nih.gov/pubmed/20729296
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq355
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