APA (7th ed.) Citation

Marchionni, E., Mannucci, L., Di Tommaso, S., Nardone, A. M., Albanese, M., Novelli, A., . . . Novelli, G. (2025). Unexpected genomic architecture in a sporadic case of C1-INH Hereditary Angioedema: The hidden heritability. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-025-04092-6

Chicago Style (17th ed.) Citation

Marchionni, Enrica, Liliana Mannucci, Silvia Di Tommaso, Anna Maria Nardone, Maria Albanese, Antonio Novelli, Federica Carla Sangiuolo, Paola Triggianese, and Giuseppe Novelli. "Unexpected Genomic Architecture in a Sporadic Case of C1-INH Hereditary Angioedema: The Hidden Heritability." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-025-04092-6.

MLA (9th ed.) Citation

Marchionni, Enrica, et al. "Unexpected Genomic Architecture in a Sporadic Case of C1-INH Hereditary Angioedema: The Hidden Heritability." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-025-04092-6.