학술논문
A rare autosomal dominant variant in regulator of calcineurin type 1 (RCAN1) gene confers enhanced calcineurin activity and may cause FSGS
Document Type
Article
Author
Lane, B.M.; Chryst-Stangl, M.; Wu, G.; Gbadegesin, R.; Murray, S.; Conlon, S.; Conlon, P.J.; Benson, K.; Cavalleri, G.; Bierzynska, A.; Saleem, M.; Wang, L.; Spurney, R.; Doyle, B.; Fennelly, N.; Dorman, A.; Vega-Warner, V.; Fermin, D.; Vijayan, P.; Qureshi, M.A.; Barua, M.; Shril, S.; Hildebrandt, F.; Sampson, M.G.; Pollak, M.; Howell, D.
Source
In: Journal of the American Society of Nephrology . (Journal of the American Society of Nephrology, July 2021, 32(7):1682-1695)
Subject
Language
English
ISSN
15333450
10466673
10466673