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1 Ergebnisse
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Bi-allelic loss-of-function variants in KIF21A cause severe..:
Falb, Ruth J
;
Müller, Amelie J
;
Klein, Wolfram
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811090/. , 2023
Link:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811090/
RT Journal T1
Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex
UL https://suche.suub.uni-bremen.de/peid=base-ftpubmed:oai:pubmedcentral.nih.gov:9811090&Exemplar=1&LAN=DE A1 Falb, Ruth J A1 Müller, Amelie J A1 Klein, Wolfram A1 Grimmel, Mona A1 Grasshoff, Ute A1 Spranger, Stephanie A1 Stöbe, Petra A1 Gauck, Darja A1 Kuechler, Alma A1 Dikow, Nicola A1 Schwaibold, Eva M C A1 Schmidt, Christoph A1 Averdunk, Luisa A1 Buchert, Rebecca A1 Heinrich, Tilman A1 Prodan, Natalia A1 Park, Joohyun A1 Kehrer, Martin A1 Sturm, Marc A1 Kelemen, Olga A1 Hartmann, Silke A1 Horn, Denise A1 Emmerich, Dirk A1 Hirt, Nina A1 Neumann, Armin A1 Kristiansen, Glen A1 Gembruch, Ulrich A1 Haen, Susanne A1 Siebert, Reiner A1 Hentze, Sabine A1 Hoopmann, Markus A1 Ossowski, Stephan A1 Waldmüller, Stephan A1 Beck-Wödl, Stefanie A1 Gläser, Dieter A1 Tekesin, Ismail A1 Distelmaier, Felix A1 Riess, Olaf A1 Kagan, Karl-Oliver A1 Dufke, Andreas A1 Haack, Tobias B PB BMJ Publishing Group YR 2023 K1 Novel Disease Loci JF http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811090/ LK http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811090/ DO http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811090/ SF ELIB - SuUB Bremen
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