MO030 : Familial clustering of a rare UMOD variant in undiagnosed hereditary nephropathy suggests the presence of a common ancestral founder mutation

Chung, N.K.X., Valluru, M., Butland, L. et al. (3 more authors) (2022) MO030 : Familial clustering of a rare UMOD variant in undiagnosed hereditary nephropathy suggests the presence of a common ancestral founder mutation. In: Nephrology Dialysis Transplantation. 59th ERA Congress, 19-22 May 2022, Paris, France (and virtual). Oxford University Press

Metadata

Item Type: Proceedings Paper
Authors/Creators:
Copyright, Publisher and Additional Information:

© 2022 The Author(s).
Keywords: Genetic Testing; Genetics; Kidney Disease; Human Genome; Clinical Research; 2.1 Biological and endogenous factors; Renal and urogenital
Dates:
  • Published (online): 3 May 2022
  • Published: 3 May 2022
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Sheffield Teaching Hospitals
Depositing User: Symplectic Sheffield
Date Deposited: 16 May 2022 11:31
Last Modified: 16 May 2022 11:31
Status: Published
Publisher: Oxford University Press
Refereed: Yes
Identification Number: 10.1093/ndt/gfac062.011
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Open Archives Initiative ID (OAI ID):

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