Items where authors include "Chung, N.K.X."

Article

Valluru, M.K. orcid.org/0000-0001-9156-866X, Chung, N.K.X., Gilchrist, M. et al. (6 more authors) (2022) A founder UMOD variant is a common cause of hereditary nephropathy in the British population. Journal of Medical Genetics. ISSN 0022-2593

Chung, N.K.X., Metherall, P., McCormick, J.A. et al. (2 more authors) (2022) Individualized everolimus treatment for tuberous sclerosis-related angiomyolipoma promotes treatment adherence and response. Clinical Kidney Journal, 15 (6). pp. 1160-1168. ISSN 2048-8505

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 .