Acquaviva, F.; Bruno, G.; Palladino, F.; Rubino, A.; Russo, C.; Pandolfi, M.; Covelli, E.M.; Evangelista, E.; De Falco, L.; Tirozzi, A.;
et al. Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in SOST Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature. Int. J. Mol. Sci. 2025, 26, 8175.
https://doi.org/10.3390/ijms26178175
AMA Style
Acquaviva F, Bruno G, Palladino F, Rubino A, Russo C, Pandolfi M, Covelli EM, Evangelista E, De Falco L, Tirozzi A,
et al. Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in SOST Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature. International Journal of Molecular Sciences. 2025; 26(17):8175.
https://doi.org/10.3390/ijms26178175
Chicago/Turabian Style
Acquaviva, Fabio, Giorgia Bruno, Federica Palladino, Alfonso Rubino, Carmela Russo, Maria Pandolfi, Eugenio Maria Covelli, Eloisa Evangelista, Luigia De Falco, Alfonsina Tirozzi,
and et al. 2025. "Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in SOST Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature" International Journal of Molecular Sciences 26, no. 17: 8175.
https://doi.org/10.3390/ijms26178175
APA Style
Acquaviva, F., Bruno, G., Palladino, F., Rubino, A., Russo, C., Pandolfi, M., Covelli, E. M., Evangelista, E., De Falco, L., Tirozzi, A., De Brasi, D., & Varone, A.
(2025). Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in SOST Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature. International Journal of Molecular Sciences, 26(17), 8175.
https://doi.org/10.3390/ijms26178175
