In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2

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In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2

Author: Morison, Lottie D.; Meffert, Elisabeth; Stampfer, Miriam; Steiner-Wilke, Irene; Vollmer, Brigitte; Schulze, Katrin; Briggs, Tracy; Braden, Ruth; Vogel, Adam; Thompson-Lake, Daisy; Patel, Chirag; Blair, Edward; Goel, Himanshu; Turner, Samantha; Moog, Ute; Riess, Angelika; Liegeois, Frederique; Koolen, David A.; Amor, David J.; Kleefstra, Tjitske; Fisher, Simon E.; Zweier, Christiane; Morgan, Angela T.
Tübinger Autor(en):
Steiner-Wilke, Irene
Riess, Angelika
Published in: Journal of Medical Genetics (2023), Bd. 60, H. 6, S. 597-607
Verlagsangabe: London : Bmj Publishing Group
Language: English
Full text: http://dx.doi.org/10.1136/jmg-2022-108734
ISSN: 0022-2593
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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