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....

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Detalles Bibliográficos
Autores principales: Roberts, Neil A., Woolf, Adrian S., Stuart, Helen M., Thuret, Raphaël, McKenzie, Edward A., Newman, William G., Hilton, Emma N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Articles
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

Internet

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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