Associated Papers
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.
Estruch SB et al.
Human Molecular Genetics, 2018
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.
Estruch SB et al.
Journal of Neurodevelopmental Disorders, 2016
Neurogenomics of speech and language disorders: the road ahead.
Deriziotis P et al.
Genome Biology, 2013
[Genetic factors in the development of language].
Sanjuán J et al.
Revista De Neurologia, 2010
Unravelling neurogenetic networks implicated in developmental language disorders.
Vernes SC et al.
Biochemical Society Transactions, 2009
Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2.
Tomblin JB et al.
Journal of Speech, Language, and Hearing Research : Jslhr, 2009
Functional genetic analysis of mutations implicated in a human speech and language disorder.
Vernes SC et al.
Human Molecular Genetics, 2006
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
MacDermot KD et al.
American Journal of Human Genetics, 2005
[FOXP2 and the molecular biology of language: new evidence. I. Phenotypic aspects and animal models].
Benítez-Burraco A
Revista De Neurologia, 0
Select a paper to view details