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Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome.
J Am Soc Nephrol. 2021 Mar;32(3):580-596. doi: 10.1681/ASN.2020040490. Epub 2021 Feb 16.
J Am Soc Nephrol. 2021.
PMID: 33593823
Free PMC article.
Galloway-Mowat syndrome: New insights from bioinformatics and expression during Xenopus embryogenesis.
Treimer E, Niedermayer K, Schumann S, Zenker M, Schmeisser MJ, Kühl SJ.
Treimer E, et al.
Gene Expr Patterns. 2021 Dec;42:119215. doi: 10.1016/j.gep.2021.119215. Epub 2021 Oct 4.
Gene Expr Patterns. 2021.
PMID: 34619372
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Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome.
Treimer E, Kalayci T, Schumann S, Suer I, Greco S, Schanze D, Schmeisser MJ, Kühl SJ, Zenker M.
Treimer E, et al.
Hum Mutat. 2022 Dec;43(12):1866-1871. doi: 10.1002/humu.24472. Epub 2022 Sep 27.
Hum Mutat. 2022.
PMID: 36116039
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