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bibliographicCitation Peretz I, Ross J, Bourassa CV, Perreault LL, Dion PA, Weiss MW, Felezeu M, Rouleau GA, Dubé M. 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. 2022 Aug 18;1517(1):279–85. doi: 10.1111/nyas.14883.
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title Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?
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