De Paolis, E.; Raspaglio, G.; Ciferri, N.; Zangrilli, I.; Ricciardi Tenore, C.; Urbani, A.; Ferraro, P.M.; Minucci, A.; Concolino, P.
Single-Base Substitution Causing Dual-Exon Skipping Event in PKD2 Gene: Unusual Molecular Finding from Exome Sequencing in a Patient with Autosomal Dominant Polycystic Kidney Disease. J. Clin. Med. 2024, 13, 4682.
https://doi.org/10.3390/jcm13164682
AMA Style
De Paolis E, Raspaglio G, Ciferri N, Zangrilli I, Ricciardi Tenore C, Urbani A, Ferraro PM, Minucci A, Concolino P.
Single-Base Substitution Causing Dual-Exon Skipping Event in PKD2 Gene: Unusual Molecular Finding from Exome Sequencing in a Patient with Autosomal Dominant Polycystic Kidney Disease. Journal of Clinical Medicine. 2024; 13(16):4682.
https://doi.org/10.3390/jcm13164682
Chicago/Turabian Style
De Paolis, Elisa, Giuseppina Raspaglio, Nunzia Ciferri, Ilaria Zangrilli, Claudio Ricciardi Tenore, Andrea Urbani, Pietro Manuel Ferraro, Angelo Minucci, and Paola Concolino.
2024. "Single-Base Substitution Causing Dual-Exon Skipping Event in PKD2 Gene: Unusual Molecular Finding from Exome Sequencing in a Patient with Autosomal Dominant Polycystic Kidney Disease" Journal of Clinical Medicine 13, no. 16: 4682.
https://doi.org/10.3390/jcm13164682
APA Style
De Paolis, E., Raspaglio, G., Ciferri, N., Zangrilli, I., Ricciardi Tenore, C., Urbani, A., Ferraro, P. M., Minucci, A., & Concolino, P.
(2024). Single-Base Substitution Causing Dual-Exon Skipping Event in PKD2 Gene: Unusual Molecular Finding from Exome Sequencing in a Patient with Autosomal Dominant Polycystic Kidney Disease. Journal of Clinical Medicine, 13(16), 4682.
https://doi.org/10.3390/jcm13164682
