Stellacci, E.; Niceta, M.; Bruselles, A.; Straface, E.; Tatti, M.; Carvetta, M.; Mancini, C.; Cecchetti, S.; Parravano, M.; Barbano, L.;
et al. Whole Genome Sequencing Solves an Atypical Form of Bardet–Biedl Syndrome: Identification of Novel Pathogenic Variants of BBS9. Int. J. Mol. Sci. 2024, 25, 8313.
https://doi.org/10.3390/ijms25158313
AMA Style
Stellacci E, Niceta M, Bruselles A, Straface E, Tatti M, Carvetta M, Mancini C, Cecchetti S, Parravano M, Barbano L,
et al. Whole Genome Sequencing Solves an Atypical Form of Bardet–Biedl Syndrome: Identification of Novel Pathogenic Variants of BBS9. International Journal of Molecular Sciences. 2024; 25(15):8313.
https://doi.org/10.3390/ijms25158313
Chicago/Turabian Style
Stellacci, Emilia, Marcello Niceta, Alessandro Bruselles, Emilio Straface, Massimo Tatti, Mattia Carvetta, Cecilia Mancini, Serena Cecchetti, Mariacristina Parravano, Lucilla Barbano,
and et al. 2024. "Whole Genome Sequencing Solves an Atypical Form of Bardet–Biedl Syndrome: Identification of Novel Pathogenic Variants of BBS9" International Journal of Molecular Sciences 25, no. 15: 8313.
https://doi.org/10.3390/ijms25158313
APA Style
Stellacci, E., Niceta, M., Bruselles, A., Straface, E., Tatti, M., Carvetta, M., Mancini, C., Cecchetti, S., Parravano, M., Barbano, L., Varano, M., Tartaglia, M., Ziccardi, L., & Cordeddu, V.
(2024). Whole Genome Sequencing Solves an Atypical Form of Bardet–Biedl Syndrome: Identification of Novel Pathogenic Variants of BBS9. International Journal of Molecular Sciences, 25(15), 8313.
https://doi.org/10.3390/ijms25158313
