Evaluation of the ISL1 gene in the pathogenesis of bladder exstrophy in a Swedish cohort

Bladder exstrophy is a congenital closure defect of the urinary bladder with a profound effect on morbidity. Although the malformation is usually sporadic, a genetic background is supported by an increased recurrence risk in relatives, higher concordance rates in monozygotic twins and several associ...

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Detalles Bibliográficos
Autores principales: Arkani, Samara, Cao, Jia, Lundin, Johanna, Nilsson, Daniel, Källman, Thomas, Barker, Gillian, Holmdahl, Gundela, Clementsson Kockum, Christina, Matsson, Hans, Nordenskjöld, Agneta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874392/
https://www.ncbi.nlm.nih.gov/pubmed/29619236
http://dx.doi.org/10.1038/hgv.2018.9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874392/
https://www.ncbi.nlm.nih.gov/pubmed/29619236
http://dx.doi.org/10.1038/hgv.2018.9

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