A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity

Vesicoureteral reflux (VUR) is the most common disease of the urinary tract in children. In order to identify gene(s) involved in this complex disorder, we performed a genome-wide search in a selected sample of 31 patients with primary VUR from eight families originating from southern Italy. Sixteen...

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Detalhes bibliográficos
Main Authors: Conte, Maria Luisa, Bertoli-Avella, Aida M., de Graaf, Bianca M., Punzo, Francesca, Lama, Giuliana, La Manna, Angela, Grassia, Carolina, Rambaldi, Pier Francesco, Oostra, Ben A., Perrotta, Silverio
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2008
Assuntos:
Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2259258/
https://ncbi.nlm.nih.gov/pubmed/18197425
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-007-0675-z
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