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