Christodoulaki, V.; Kosma, K.; Marinakis, N.M.; Tilemis, F.-N.; Stergiou, N.; Kampouraki, A.; Kapogiannis, C.; Karava, V.; Mitsioni, A.; Mila, M.;
et al. Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children. Genes 2024, 15, 1016.
https://doi.org/10.3390/genes15081016
AMA Style
Christodoulaki V, Kosma K, Marinakis NM, Tilemis F-N, Stergiou N, Kampouraki A, Kapogiannis C, Karava V, Mitsioni A, Mila M,
et al. Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children. Genes. 2024; 15(8):1016.
https://doi.org/10.3390/genes15081016
Chicago/Turabian Style
Christodoulaki, Vasileia, Konstantina Kosma, Nikolaos M. Marinakis, Faidon-Nikolaos Tilemis, Nikolaos Stergiou, Afroditi Kampouraki, Charalampos Kapogiannis, Vasiliki Karava, Andromachi Mitsioni, Maria Mila,
and et al. 2024. "Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children" Genes 15, no. 8: 1016.
https://doi.org/10.3390/genes15081016
APA Style
Christodoulaki, V., Kosma, K., Marinakis, N. M., Tilemis, F.-N., Stergiou, N., Kampouraki, A., Kapogiannis, C., Karava, V., Mitsioni, A., Mila, M., Kanaka-Gantenbein, C., Makrythanasis, P., Tzetis, M., & Traeger-Synodinos, J.
(2024). Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children. Genes, 15(8), 1016.
https://doi.org/10.3390/genes15081016
