FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum

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FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum

Author: Reuter, Miriam S.; Riess, Angelika; Moog, Ute; Briggs, Tracy A.; Chandler, Kate E.; Rauch, Anita; Stampfer, Miriam; Steindl, Katharina; Glaeser, Dieter; Joset, Pascal; Krumbiegel, Mandy; Rabe, Harald; Schulte-Mattler, Uta; Bauer, Peter; Beck-Woedl, Stefanie; Kohlhase, Juergen; Reis, Andre; Zweier, Christiane
Tübinger Autor(en):
Stampfer, Miriam
Bauer, Peter
Rieß, Angelika
Beck-Wödl, Stefanie
Published in: Journal of Medical Genetics (2017), Bd. 54, H. 1, S. 64-72
Verlagsangabe: Bmj Publishing Group
Language: English
Full text: http://dx.doi.org/10.1136/jmedgenet-2016-104094
ISSN: 1468-6244
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
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