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

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

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

Autor(en):

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

Erschienen in:

Journal of Medical Genetics (2017), Bd. 54, H. 1, S. 64-72

Verlagsangabe:

Bmj Publishing Group

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1136/jmedgenet-2016-104094

ISSN:

1468-6244