RYK is not mutated in autosomal dominant Robinow syndrome
- PMID: 23355721
- PMCID: PMC3554954
- DOI: 10.1074/jbc.L112.439489
RYK is not mutated in autosomal dominant Robinow syndrome
Comment in
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Reply to Mazzeu: Human mutations in RYK might cause Robinow syndrome.J Biol Chem. 2013 Jan 25;288(4):2906. doi: 10.1074/jbc.l112.444539. J Biol Chem. 2013. PMID: 23472253 Free PMC article. No abstract available.
Comment on
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The Wnt coreceptor Ryk regulates Wnt/planar cell polarity by modulating the degradation of the core planar cell polarity component Vangl2.J Biol Chem. 2012 Dec 28;287(53):44518-25. doi: 10.1074/jbc.M112.414441. Epub 2012 Nov 9. J Biol Chem. 2012. PMID: 23144463 Free PMC article.
References
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- Halford M. M., Armes J., Buchert M., Meskenaite V., Grail D., Hibbs M. L., Wilks A. F., Farlie P. G., Newgreen D. F., Hovens C. M., Stacker S. A. (2000) Ryk-deficient mice exhibit craniofacial defects associated with perturbed Eph receptor crosstalk. Nat. Genet. 25, 414–418 - PubMed
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