Lack of phosphomannomutase 2 affects Xenopus laevis morphogenesis and the non-canonical Wnt5a/Ror2 signalling
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-015-9874-0
Reference50 articles.
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3. Bokhoven VH, Celli J, Kayserili H et al (2000) Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome. Nat Genet 25:423–426
4. Brunetti-Pierri N, Del Gaudio D, Peters H et al (2008) Robinow syndrome: phenotypic variability in a family with a novel intragenic ROR2 mutation. Am J Med Genet 146A:2804–2809
5. Buttler K, Becker J, Pukrop T et al (2013) Maldevelopment of dermal lymphatics in Wnt5a-knockout-mice. Dev Biol 381:365–376
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