APA (7th ed.) Citation

S, C., T, R., T, B., S, B., P, B., F, E., . . . S, M. (2026). Dystonia-deafness syndrome 1 caused by ACTB p.(Arg183Trp) de novo variant: One novel case extending the phenotypic spectrum. Neurogenetics, 27(1), 6. https://doi.org/10.1007/s10048-025-00875-y

Chicago Style (17th ed.) Citation

S, Cuinat, et al. "Dystonia-deafness Syndrome 1 Caused by ACTB P.(Arg183Trp) De Novo Variant: One Novel Case Extending the Phenotypic Spectrum." Neurogenetics 27, no. 1 (2026): 6. https://doi.org/10.1007/s10048-025-00875-y.

MLA (9th ed.) Citation

S, Cuinat, et al. "Dystonia-deafness Syndrome 1 Caused by ACTB P.(Arg183Trp) De Novo Variant: One Novel Case Extending the Phenotypic Spectrum." Neurogenetics, vol. 27, no. 1, 2026, p. 6, https://doi.org/10.1007/s10048-025-00875-y.