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Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syn..:
Mann, Nina
;
Mzoughi, Slim
;
Schneider, Ronen
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920168/. , 2021
Link:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920168/
RT Journal T1
Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftpubmed:oai:pubmedcentral.nih.gov:7920168&Exemplar=1&LAN=DE A1 Mann, Nina A1 Mzoughi, Slim A1 Schneider, Ronen A1 Kühl, Susanne J A1 Schanze, Denny A1 Klämbt, Verena A1 Lovric, Svjetlana A1 Mao, Youying A1 Shi, Shasha A1 Tan, Weizhen A1 Kühl, Michael A1 Onuchic-Whitford, Ana C A1 Treimer, Ernestine A1 Kitzler, Thomas M A1 Kause, Franziska A1 Schumann, Sven A1 Nakayama, Makiko A1 Buerger, Florian A1 Shril, Shirlee A1 van der Ven, Amelie T A1 Majmundar, Amar J A1 Holton, Kristina Marie A1 Kolb, Amy A1 Braun, Daniela A A1 Rao, Jia A1 Jobst-Schwan, Tilman A1 Mildenberger, Eva A1 Lennert, Thomas A1 Kuechler, Alma A1 Wieczorek, Dagmar A1 Gross, Oliver A1 Ermisch-Omran, Beate A1 Werberger, Anja A1 Skalej, Martin A1 Janecke, Andreas R A1 Soliman, Neveen A A1 Mane, Shrikant M A1 Lifton, Richard P A1 Kadlec, Jan A1 Guccione, Ernesto A1 Schmeisser, Michael J A1 Zenker, Martin A1 Hildebrandt, Friedhelm PB American Society of Nephrology YR 2021 K1 Basic Research JF http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920168/ LK http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920168/ DO http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920168/ SF ELIB - SuUB Bremen
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