TY  - GEN
AU  - Sollis,Elliot
AU  - Graham,Sarah A
AU  - Vino,Arianna
AU  - Froehlich,Henning
AU  - Vreeburg,Maaike
AU  - Dimitropoulou,Danai
AU  - Gilissen,Christian
AU  - Pfundt,Rolph
AU  - Rappold,Gudrun A
AU  - Brunner,Han G
AU  - Deriziotis,Pelagia
AU  - Fisher,Simon E
TI  - Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder
SN  - 1460-2083
PY  - 2016///1213
KW  - Adolescent
KW  - Base Sequence
KW  - Child
KW  - DNA
KW  - genetics
KW  - Developmental Disabilities
KW  - Exome
KW  - Female
KW  - Forkhead Transcription Factors
KW  - Gene Expression Regulation
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Hypertelorism
KW  - Intellectual Disability
KW  - Language Development Disorders
KW  - Male
KW  - Molecular Sequence Data
KW  - Mutation, Missense
KW  - Pedigree
KW  - Protein Binding
KW  - Repressor Proteins
KW  - Signal Transduction
KW  - Transcription, Genetic
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/hmg/ddv495
ER  -