[HTML][HTML] An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
Mutations in the human FOXP2 gene cause impaired speech development and linguistic
deficits, which have been best characterised in a large pedigree called the KE family. The …
deficits, which have been best characterised in a large pedigree called the KE family. The …
[引用][C] An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
CA French, X Jin, TG Campbell, E Gerfen… - Molecular …, 2011 - cir.nii.ac.jp
[HTML][HTML] An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
CA French, X Jin, TG Campbell, E Gerfen… - Molecular …, 2012 - ncbi.nlm.nih.gov
Mutations in the human FOXP2 gene cause impaired speech development and linguistic
deficits, which have been best characterised in a large pedigree called the KE family. The …
deficits, which have been best characterised in a large pedigree called the KE family. The …
An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
CA French, X Jin, TG Campbell, E Gerfen… - Molecular …, 2012 - go.gale.com
Mutations in the human FOXP2 gene cause impaired speech development and linguistic
deficits, which have been best characterised in a large pedigree called the KE family. The …
deficits, which have been best characterised in a large pedigree called the KE family. The …
An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning.
CA French, X Jin, TG Campbell, E Gerfen… - Molecular …, 2011 - europepmc.org
Mutations in the human FOXP2 gene cause impaired speech development and linguistic
deficits, which have been best characterised in a large pedigree called the KE family. The …
deficits, which have been best characterised in a large pedigree called the KE family. The …
[引用][C] An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
CA FRENCH, X JIN, TG CAMPBELL… - Molecular …, 2012 - pascal-francis.inist.fr
An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during
skill learning CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic …
skill learning CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic …
[PDF][PDF] An Aetiological Foxp2 Mutation Causes Aberrant Striatal Activity and Alters Plasticity during Skill Learning
CA French, X Jin, TG Campbell, E Gerfen, M Groszer… - academia.edu
Mutations in the human FOXP2 gene cause impaired speech development and linguistic
deficits, which have been best characterized in a large pedigree called the KE family. The …
deficits, which have been best characterized in a large pedigree called the KE family. The …
[PDF][PDF] An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
CA French, X Jin, TG Campbell, E Gerfen… - Molecular …, 2011 - researchgate.net
Mutations in the human FOXP2 gene cause impaired speech development and linguistic
deficits, which have been best characterised in a large pedigree called the KE family. The …
deficits, which have been best characterised in a large pedigree called the KE family. The …
An Aetiological Mutation Causes Aberrant Striatal Activity and Alters Plasticity during Skill Learning
RM Costa, CA French, X Jin, TG Campbell… - Molecular …, 2011 - hal.science
Mutations in the human gene cause impaired speech development and linguistic deficits,
which have been best characterized in a large pedigree called the KE family. The encoded …
which have been best characterized in a large pedigree called the KE family. The encoded …
[PDF][PDF] An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
CA French, X Jin, TG Campbell, E Gerfen… - Molecular …, 2012 - cyberleninka.org
Mutations in the human FOXP2 gene cause impaired speech development and linguistic
deficits, which have been best characterised in a large pedigree called the KE family. The …
deficits, which have been best characterised in a large pedigree called the KE family. The …