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Functional characterization of a novel TP53RK mutation iden..:
Treimer, Ernestine
;
Kalayci, Tugba
;
Schumann, Sven
...
https://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fhumu.24472&file=humu24472-sup-0001-Supp_Mat.pdf. , 2023
Link:
https://doi.org/10.18725/OPARU-47137
RT Journal T1 <Title>Functional characterization of a novel TP53RK mutation identified in a family with Galloway–Mowat syndrome</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftunivulm:oai:oparu.uni-ulm.de:123456789_47213&Exemplar=1&LAN=DE A1 Treimer, Ernestine A1 Kalayci, Tugba A1 Schumann, Sven A1 Suer, Ilknur A1 Greco, Sara A1 Schanze, Denny A1 Schmeisser, Michael J A1 Kühl, Susanne J A1 Zenker, Martin PB Universität Ulm YR 2023 K1 disease modeling K1 KEOPS complex K1 TP53RK K1 DDC 540 / Chemistry & allied sciences K1 Microcephaly K1 Nephrotic syndrome K1 Mikrozephalie K1 Nephrotisches Syndrom JF https://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fhumu.24472&file=humu24472-sup-0001-Supp_Mat.pdf LK http://dx.doi.org/https://doi.org/10.18725/OPARU-47137 DO https://doi.org/10.18725/OPARU-47137 SF ELIB - SuUB Bremen
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