chromosomal translocation t(5;7)(q22;q31.2)

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Introduction

Chromosomal translocation t(5;7)(q22;q31.2) disrupting FOXP2 is a cause of severe speech & language impairment

More general terms

References

  1. ↑ UniProt http://www.uniprot.org/uniprot/O15409.html
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