Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder

Mutations in leucine-rich-repeats and immunoglobulin-like-domains 2 (LRIG2) or in heparanase 2 (HPSE2) cause urofacial syndrome, a devastating autosomal recessive disease of functional bladder outlet obstruction. It has been speculated that urofacial syndrome has a neural basis, but it is unknown wh...

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Detalles Bibliográficos
Autores principales: Roberts, Neil A., Hilton, Emma N., Lopes, Filipa M., Singh, Subir, Randles, Michael J., Gardiner, Natalie J., Chopra, Karl, Coletta, Riccardo, Bajwa, Zunera, Hall, Robert J., Yue, Wyatt W., Schaefer, Franz, Weber, Stefanie, Henriksson, Roger, Stuart, Helen M., Hedman, Håkan, Newman, William G., Woolf, Adrian S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6481288/
https://www.ncbi.nlm.nih.gov/pubmed/30885509
http://dx.doi.org/10.1016/j.kint.2018.11.040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6481288/
https://www.ncbi.nlm.nih.gov/pubmed/30885509
http://dx.doi.org/10.1016/j.kint.2018.11.040

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