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Whole-Exome Sequencing Identifies Causative Mutations in Families With Congenital Anomalies of the Kidney and Urinary Tract

Journal of the American Society of Nephrology : JASN - United States
doi 10.1681/asn.2017121265
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Abstract

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Categories
MedicineNephrology
Date

August 24, 2018

Authors
Amelie T. van der VenDervla M. ConnaughtonHadas ItyelNina MannMakiko NakayamaJing ChenAsaf VivanteDaw-yang HwangJulian SchulzDaniela A. BraunJohanna Magdalena SchmidtDavid SchapiroRonen SchneiderJillian K. WarejkoAnkana DagaAmar J. MajmundarWeizhen TanTilman Jobst-SchwanTobias HermleEugen WidmeierShazia AshrafAli AmarCharlotte A. HoogstraatenHannah HugoThomas M. KitzlerFranziska KauseCaroline M. KolvenbachRufeng DaiLeslie SpaneasKassaundra AmannDeborah R. SteinMichelle A. BaumMichael J.G. SomersNancy M. RodigMichael A. FergusonAvram Z. TraumGhaleb H. DaoukRadovan BogdanovićNatasa StajićNeveen A. SolimanJameela A. KariSherif El DesokyHanan M. FathyDanko MilosevicMuna Al-SaffarHazem S. AwadLoai A. EidAravind SelvinPrabha SenguttuvanSimone Sanna-CherchiHeidi L. RehmDaniel G. MacArthurMonkol LekKristen M. LaricchiaMichael W. WilsonShrikant M. ManeRichard P. LiftonRichard S. LeeStuart B. BauerWeining LuHeiko M. ReutterVelibor TasicShirlee ShrilFriedhelm Hildebrandt
Publisher

American Society of Nephrology (ASN)

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