#2613 Clinical spectrum and prognosis of the atypical polycystic kidney disease caused by monoallelic loss-of-function IFT140 variants

Metadata

Item Type:	Proceedings Paper
Authors/Creators:	Zagorec, N. Calamel, A. Ars, E. Ong, A. https://orcid.org/0000-0002-7211-5400 Halbritter, J. Audrezet, M.-P. Pillay, V.-G. Meur, Y.L. Sayer, J. Genkyst Study Group Gall, E.C.-L.
Copyright, Publisher and Additional Information:	© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.
Keywords:	Biomedical and Clinical Sciences; Clinical Sciences; Genetics; Kidney Disease; Clinical Research; Human Genome; Congenital Structural Anomalies; Genetic Testing; Polycystic Kidney Disease; Pediatric; 2 Aetiology; Discovery and preclinical testing of markers and technologies; Biological and endogenous factors; Detection, screening and diagnosis; Renal and urogenital; Good Health and Well Being
Dates:	Published (online): 23 May 2024 Published: May 2024
Institution:	The University of Sheffield
Academic Units:	The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Medicine and Population Health
Depositing User:	Symplectic Sheffield
Date Deposited:	03 Jul 2024 14:12
Last Modified:	03 Jul 2024 14:12
Status:	Published
Publisher:	Oxford University Press (OUP)
Refereed:	Yes
Identification Number:	10.1093/ndt/gfae069.119
Related URLs:	Conference
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Open Archives Initiative ID (OAI ID):	oai:eprints.whiterose.ac.uk:214360

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