학술논문
Mutations in PRDM15 are a novel cause of galloway-mowat syndrome
Document Type
Article
Author
Mann, N.; Schneider, R.; Klämbt, V.; Lovric, S.; Mao, Y.; Tan, W.; Onuchic-Whitford, A.C.; Kitzler, T.M.; Kause, F.; Nakayama, M.; Buerger, F.; Shril, S.; van der Ven, A.T.; Majmundar, A.J.; Kolb, A.; Braun, D.A.; Rao, J.; Jobst-Schwan, T.; Hildebrandt, F.; Mzoughi, S.; Guccione, E.; Kühl, S.J.; Kühl, M.; Werberger, A.; Schanze, D.; Zenker, M.; Shi, S.; Kadlec, J.; Treimer, E.; Schumann, S.; Schmeisser, M.J.; Holton, K.M.; Mildenberger, E.; Lennert, T.; Kuechler, A.; Wieczorek, D.; Gross, O.; Ermisch-Omran, B.; Skalej, M.; Janecke, A.R.; Soliman, N.A.; Mane, S.M.; Lifton, R.P.
Source
In: Journal of the American Society of Nephrology . (Journal of the American Society of Nephrology, March 2021, 32(3):580-596)
Subject
Language
English
ISSN
15333450
10466673
10466673