TY  - GEN
AU  - Hamdan,Fadi F
AU  - Daoud,Hussein
AU  - Rochefort,Daniel
AU  - Piton,Amélie
AU  - Gauthier,Julie
AU  - Langlois,Mathieu
AU  - Foomani,Gila
AU  - Dobrzeniecka,Sylvia
AU  - Krebs,Marie-Odile
AU  - Joober,Ridha
AU  - Lafrenière,Ronald G
AU  - Lacaille,Jean-Claude
AU  - Mottron,Laurent
AU  - Drapeau,Pierre
AU  - Beauchamp,Miriam H
AU  - Phillips,Michael S
AU  - Fombonne,Eric
AU  - Rouleau,Guy A
AU  - Michaud,Jacques L
TI  - De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment
SN  - 1537-6605
PY  - 2011///0124
KW  - Adolescent
KW  - Amino Acid Sequence
KW  - Child
KW  - Child Development Disorders, Pervasive
KW  - genetics
KW  - Child, Preschool
KW  - Female
KW  - Forkhead Transcription Factors
KW  - Humans
KW  - Intellectual Disability
KW  - Language Disorders
KW  - Male
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Repressor Proteins
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajhg.2010.09.017
ER  -