APA (7th ed.) Citation

M, C., P, G., A, R., G, A., A, B., C, B., . . . V, D. S. (2026). Deep Phenotyping of F64L Mutation in a Multicentric Cohort of Patisiran-Treated Hereditary Transthyretin Amyloidosis Patients (Patisiranitaly). European journal of neurology, 33(6), e70657. https://doi.org/10.1111/ene.70657

Chicago Style (17th ed.) Citation

M, Ceccanti, et al. "Deep Phenotyping of F64L Mutation in a Multicentric Cohort of Patisiran-Treated Hereditary Transthyretin Amyloidosis Patients (Patisiranitaly)." European Journal of Neurology 33, no. 6 (2026): e70657. https://doi.org/10.1111/ene.70657.

MLA (9th ed.) Citation

M, Ceccanti, et al. "Deep Phenotyping of F64L Mutation in a Multicentric Cohort of Patisiran-Treated Hereditary Transthyretin Amyloidosis Patients (Patisiranitaly)." European Journal of Neurology, vol. 33, no. 6, 2026, p. e70657, https://doi.org/10.1111/ene.70657.