Bibliography

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2022
Peretz I, Ross J, Bourassa CV, Perreault L-PLemieux, Dion PA, Weiss MW, Felezeu M, Rouleau GA, Dubé M-P.  2022.  Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia? Annals of the New York Academy of Sciences.