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Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus
Urofacial syndrome (UFS; previously Ochoa syndrome) is an autosomal recessive disease characterized by incomplete bladder emptying during micturition. This is associated with a dyssynergia in which the urethral walls contract at the same time as the detrusor smooth muscle in the body of the bladder....
Autores principales: | Roberts, Neil A., Woolf, Adrian S., Stuart, Helen M., Thuret, Raphaël, McKenzie, Edward A., Newman, William G., Hilton, Emma N. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103677/ https://www.ncbi.nlm.nih.gov/pubmed/24691552 http://dx.doi.org/10.1093/hmg/ddu147 |
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