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Perrault I, Hanein S, Gérard X, Mounguengue N, Bouyakoub R, Zarhrate M, Fourrage C, Jabot-Hanin F, Bocquet B, Meunier I, et al. Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic RPGRIP1 Pathologic Variant in the French Leber Congenital Amaurosis Cohort. Genes. 2021; 12(2):287. https://doi.org/10.3390/genes12020287

Perrault, Isabelle, Sylvain Hanein, Xavier Gérard, Nelson Mounguengue, Ryme Bouyakoub, Mohammed Zarhrate, Cécile Fourrage, Fabienne Jabot-Hanin, Béatrice Bocquet, Isabelle Meunier, and et al. 2021. "Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic RPGRIP1 Pathologic Variant in the French Leber Congenital Amaurosis Cohort" Genes 12, no. 2: 287. https://doi.org/10.3390/genes12020287

Perrault, I., Hanein, S., Gérard, X., Mounguengue, N., Bouyakoub, R., Zarhrate, M., Fourrage, C., Jabot-Hanin, F., Bocquet, B., Meunier, I., Zanlonghi, X., Kaplan, J., & Rozet, J.-M. (2021). Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic RPGRIP1 Pathologic Variant in the French Leber Congenital Amaurosis Cohort. Genes, 12(2), 287. https://doi.org/10.3390/genes12020287