Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment - Concepedia

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Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment

DOI Full Paper Access

187

Citations

24

References

2010

Year

Nicola Brunetti‐Pierri, Alex R. Paciorkowski, Roberto Ciccone, Erika Della Mina, María Clara Bonaglia, Renato Borgatti, Christian P. Schaaf, V. Reid Sutton, Zhilian Xia, Naftha Jelluma,

European Journal of Human Genetics

Developmental BiologyMendelian DisorderSevere Speech ImpairmentGenetic DisorderGeneticsDevelopmental EpilepsyMolecular GeneticsNeuroscienceGenomicsDisease Gene IdentificationMental RetardationMedicineNeurogenetics

References

	Year	Citations

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