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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...
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group
2018
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| Materias: | |
| 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 |