Broca’s aphasia



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Broca’s aphasia

  • Broca’s aphasia

  • Wernicke’s aphasia

  • global aphasia





An inherited deficit in spoken language has been associated with a mutation in FOXP2 gene on chromosome 7.

  • An inherited deficit in spoken language has been associated with a mutation in FOXP2 gene on chromosome 7.

  • Functional magnetic resonance imaging study has linked the deficit to underactivity in Broca's area during word generation.

  • Possible link between FOXP2 and the mirror-neuron system observed in the primate homologue of Broca's area.

  • This link might have implications for the evolution of Broca's area and its role in speech (a new gene).




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