Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment

Pía Villanueva*, Ron Nudel, Alexander Hoischen, María Angélica Fernández, Nuala H. Simpson, Christian Gilissen, Rose H. Reader, Lillian Jara, Maria Magdalena Echeverry, Clyde Francks, Gillian Baird, Gina Conti-Ramsden, Anne O’Hare, Patrick F. Bolton, Elizabeth R. Hennessy, Hernán Palomino, Luis Carvajal-Carmona, Joris A. Veltman, Jean Baptiste Cazier, Zulema De BarbieriSimon E. Fisher, Dianne F. Newbury, V. Slonims, Ann Clark, Jocelynne Watson, E. Simonoff, A. Pickles, A. Everitt, J. Seckl, H. Cowie, W. Cohen, J. Nasir, D. V M Bishop, Z. Simkin

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

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Biochemistry, Genetics and Molecular Biology