Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants.

MLA

Poncet, Anaïs F., et al. “Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants.” International Journal of Molecular Sciences, vol. 23, no. 8, Apr. 2022. EBSCOhost, https://doi.org/10.3390/ijms23084294.

APA

Poncet, A. F., Grunewald, O., Vaclavik, V., Meunier, I., Drumare, I., Pelletier, V., Bocquet, B., Todorova, M. G., Le Moing, A.-G., Devos, A., Schorderet, D. F., Jobic, F., Defoort-Dhellemmes, S., Dollfus, H., Smirnov, V. M., & Dhaenens, C.-M. (2022). Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants. International Journal of Molecular Sciences, 23(8). https://doi.org/10.3390/ijms23084294

Chicago

Poncet, Anaïs F, Olivier Grunewald, Veronika Vaclavik, Isabelle Meunier, Isabelle Drumare, Valérie Pelletier, Béatrice Bocquet, et al. 2022. “Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants.” International Journal of Molecular Sciences 23 (8). doi:10.3390/ijms23084294.