Items where authors include "Butland, L."
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Number of items: 2.
Article
Valluru, M.K. orcid.org/0000-0001-9156-866X, Chung, N.K.X., Gilchrist, M. et al. (6 more authors) (2023) A founder UMOD variant is a common cause of hereditary nephropathy in the British population. Journal of Medical Genetics, 60 (4). pp. 397-405. ISSN 0022-2593
Proceedings Paper
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 .