h1

%0 Journal Article
%A Brunet, Theresa
%A Zott, Benedikt
%A Lieftüchter, Victoria
%A Lenz, Dominic
%A Schmidt, Axel
%A Peters, Philipp
%A Kopajtich, Robert
%A Zaddach, Malin
%A Zimmermann, Hanna
%A Hüning, Irina
%A Ballhausen, Diana
%A Staufner, Christian
%A Bianzano, Alyssa
%A Hughes, Joanne
%A Taylor, Robert W.
%A McFarland, Robert
%A Devlin, Anita
%A Mihaljević, Mihaela
%A Barišić, Nina
%A Rohlfs, Meino
%A Wilfling, Sibylle
%A Sondheimer, Neal
%A Hewson, Stacy
%A Marinakis, Nikolaos M.
%A Kosma, Konstantina
%A Traeger-Synodinos, Joanne
%A Elbracht, Miriam
%A Begemann, Matthias
%A Trepels-Kottek, Sonja
%A Hasan, Dimah
%A Scala, Marcello
%A Capra, Valeria
%A Zara, Federico
%A van der Ven, Amelie T.
%A Driemeyer, Joenna
%A Apitz, Christian
%A Krämer, Johannes
%A Strong, Alanna
%A Hakonarson, Hakon
%A Watson, Deborah
%A Mayr, Johannes A.
%A Prokisch, Holger
%A Meitinger, Thomas
%A Borggraefe, Ingo
%A Spiegler, Juliane
%A Baric, Ivo
%A Paolini, Marco
%A Gerstl, Lucia
%A Wagner, Matias
%T De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke
%J Genetics in medicine
%V 26
%N 2
%@ 1530-0366
%C Amsterdam
%I Elsevier
%M RWTH-CONV-253483
%P 101013
%D 2024
%F PUB:(DE-HGF)16 ; PUB:(DE-HGF)7
%9 Journal ArticleContribution to a book
%U <Go to ISI:>//WOS:001194984300001
%$ pmid:37924258
%R 10.1016/j.gim.2023.101013
%U https://publications.rwth-aachen.de/record/1007118