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Benvenuto M, Palumbo P, Di Muro E, Perrotta CS, Mazza T, Mandarà GML, Palumbo O, Carella M. Identification of a Novel FOXP1 Variant in a Patient with Hypotonia, Intellectual Disability, and Severe Speech Impairment. Genes. 2023; 14(10):1958. https://doi.org/10.3390/genes14101958

Benvenuto, Mario, Pietro Palumbo, Ester Di Muro, Concetta Simona Perrotta, Tommaso Mazza, Giuseppa Maria Luana Mandarà, Orazio Palumbo, and Massimo Carella. 2023. "Identification of a Novel FOXP1 Variant in a Patient with Hypotonia, Intellectual Disability, and Severe Speech Impairment" Genes 14, no. 10: 1958. https://doi.org/10.3390/genes14101958

Benvenuto, M., Palumbo, P., Di Muro, E., Perrotta, C. S., Mazza, T., Mandarà, G. M. L., Palumbo, O., & Carella, M. (2023). Identification of a Novel FOXP1 Variant in a Patient with Hypotonia, Intellectual Disability, and Severe Speech Impairment. Genes, 14(10), 1958. https://doi.org/10.3390/genes14101958