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

Miriam S Reuter; Angelika Riess; Ute Moog; Tracy A Briggs; Kate E Chandler; Anita Rauch; Miriam Stampfer; Katharina Steindl; Dieter Gläser; Pascal Joset; DDD Study; Mandy Krumbiegel; Harald Rabe; Uta Schulte-Mattler; Peter Bauer; Stefanie Beck-Wödl; Jürgen Kohlhase; André Reis; Christiane Zweier

doi:10.1136/jmedgenet-2016-104094

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Original article

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

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Miriam S Reuter Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany PubMed articles Google scholar articles
Angelika Riess Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany PubMed articles Google scholar articles
Ute Moog Institute of Human Genetics, Heidelberg University, Heidelberg, Germany PubMed articles Google scholar articles
Tracy A Briggs Manchester Centre for Genomic Medicine, St Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK Faculty of Medical and Human Sciences, Institute of Human Development, University of Manchester, Manchester, UK PubMed articles Google scholar articles
Kate E Chandler Manchester Centre for Genomic Medicine, St Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK PubMed articles Google scholar articles
Anita Rauch Institute of Medical Genetics, University of Zurich, Schlieren-Zurich, Switzerland PubMed articles Google scholar articles
Miriam Stampfer Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany PubMed articles Google scholar articles
Katharina Steindl Institute of Medical Genetics, University of Zurich, Schlieren-Zurich, Switzerland PubMed articles Google scholar articles
Dieter Gläser Genetikum, Neu-Ulm, Germany PubMed articles Google scholar articles
Pascal Joset Institute of Medical Genetics, University of Zurich, Schlieren-Zurich, Switzerland PubMed articles Google scholar articles
DDD Study
Google scholar articles
Mandy Krumbiegel Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany PubMed articles Google scholar articles
Harald Rabe Kinderzentrum St. Martin, Regensburg, Germany PubMed articles Google scholar articles
Uta Schulte-Mattler Kinderzentrum St. Martin, Regensburg, Germany PubMed articles Google scholar articles
Peter Bauer Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany PubMed articles Google scholar articles
Stefanie Beck-Wödl Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany PubMed articles Google scholar articles
Jürgen Kohlhase Centre for Human Genetics, Freiburg, Germany PubMed articles Google scholar articles
André Reis Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany PubMed articles Google scholar articles
Christiane Zweier Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany PubMed articles Google scholar articles

Correspondence to Dr Christiane Zweier, Institute of Human Genetics, Friedrich-Alexander-University Erlangen-Nürnberg, Schwabachanlage 10, Erlangen 91054, Germany; christiane.zweier{at}uk-erlangen.de

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Citation

Reuter MS, Riess A, Moog U, et al

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

Journal of Medical Genetics 2017;54:64-72.

Publication history

Received June 9, 2016
Revised July 31, 2016
Accepted August 1, 2016
First published August 29, 2016.

Online issue publication

January 06, 2017

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