A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 (RLBP1) gene causes retinitis punctata albescens.

MLA

Torres-Costa, Sónia, et al. “A Novel Homozygous Frameshift Variant in the Cellular Retinaldehyde-Binding Protein 1 (RLBP1) Gene Causes Retinitis Punctata Albescens.” European Journal of Ophthalmology, vol. 31, no. 3, May 2021, pp. NP74-NP80. EBSCOhost, https://doi.org/10.1177/1120672120919064.

APA

Torres-Costa, S., Ferreira, C. S., Grangeia, A., Santos-Silva, R., Brandão, E., Estrela-Silva, S., & Falcão-Reis, F. (2021). A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 (RLBP1) gene causes retinitis punctata albescens. European Journal of Ophthalmology, 31(3), NP74-NP80. https://doi.org/10.1177/1120672120919064

Chicago

Torres-Costa, Sónia, Carla Sofia Ferreira, Ana Grangeia, Renato Santos-Silva, Elisete Brandão, Sérgio Estrela-Silva, and Fernando Falcão-Reis. 2021. “A Novel Homozygous Frameshift Variant in the Cellular Retinaldehyde-Binding Protein 1 (RLBP1) Gene Causes Retinitis Punctata Albescens.” European Journal of Ophthalmology 31 (3): NP74-NP80. doi:10.1177/1120672120919064.