Exome sequencing in an admixed isolated population indicates NFXL1 variants 
confer a risk for Specific Language Impairment

Villanueva, P.; Nudel, R.; Hoischen, A.; Fernández, M. A.; Simpson, N. H.; Gilissen, C.; Reader, R. H.; Jara, L.; Echeverry, M.M.; Francks, Clyde; Baird, G.; Conti-Ramsden, G.; O’Hare, A.; Bolton, P.F.; Hennessy, E. R.; the SLI Consortium,; Palomino, H.; Carvajal-Carmona Veltman  J.A., L.; Veltman, Joris A.; Cazier, J.-B.; De Barbieri, Z.; Fisher, Simon E.; Newbury, D.F.

doi:10.1371/journal.pgen.1004925

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Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for Specific Language Impairment

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Francks, Clyde
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;
Donders Institute for Brain, Cognition and Behaviour, External Organizations;
Imaging Genomics, MPI for Psycholinguistics, Max Planck Society;

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Fisher, Simon E.
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;
Donders Institute for Brain, Cognition and Behaviour, External Organizations;

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Villanueva, P., Nudel, R., Hoischen, A., Fernández, M. A., Simpson, N. H., Gilissen, C., et al. (2015). Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for Specific Language Impairment. PLoS Genetics, 11(3): e1004925. doi:10.1371/journal.pgen.1004925.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0025-A88C-5

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