TY  - GEN
AU  - Reuter,Miriam S
AU  - Riess,Angelika
AU  - Moog,Ute
AU  - Briggs,Tracy A
AU  - Chandler,Kate E
AU  - Rauch,Anita
AU  - Stampfer,Miriam
AU  - Steindl,Katharina
AU  - Gläser,Dieter
AU  - Joset,Pascal
AU  - Krumbiegel,Mandy
AU  - Rabe,Harald
AU  - Schulte-Mattler,Uta
AU  - Bauer,Peter
AU  - Beck-Wödl,Stefanie
AU  - Kohlhase,Jürgen
AU  - Reis,André
AU  - Zweier,Christiane
TI  - FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum
SN  - 1468-6244
PY  - 2017///1101
KW  - Developmental Disabilities
KW  - genetics
KW  - Forkhead Transcription Factors
KW  - Humans
KW  - Language Disorders
KW  - Male
KW  - Mutation, Missense
KW  - Pedigree
KW  - Point Mutation
KW  - Sequence Deletion
KW  - Speech
KW  - physiology
KW  - Speech Disorders
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1136/jmedgenet-2016-104094
ER  -