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...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	HUMAN GENOME VARIATION 2018-01, Vol.5 (1), p.18009-18009, Article 18009
Hauptverfasser:	Arkani, Samara, Cao, Jia, Lundin, Johanna, Nilsson, Daniel, Källman, Thomas, Barker, Gillian, Holmdahl, Gundela, Clementsson Kockum, Christina, Matsson, Hans, Nordenskjöld, Agneta
Format:	Artikel
Sprache:	eng
Schlagworte:	692/420/2489/144 692/699/2768/1335 Biomedical and Life Sciences Biomedicine Bladder Gene Expression Gene Function Gene Therapy Human Genetics Medicin och hälsovetenskap Molecular Genetics Molecular Medicine Molekylär genetik
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!