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An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
Foxp2 in vivo recording KE family motor-skill learning speech and language striatum
2015/4/20
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 encoded protein is highly ...