Littink, K.W.; Stappers, P.T.Y.; Riemslag, F.C.C.; Talsma, H.E.; Van Genderen, M.M.; Cremers, F.P.M.; Collin, R.W.J.; Van den Born, L.I.
Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68.
https://doi.org/10.3390/genes9020068
AMA Style
Littink KW, Stappers PTY, Riemslag FCC, Talsma HE, Van Genderen MM, Cremers FPM, Collin RWJ, Van den Born LI.
Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes. 2018; 9(2):68.
https://doi.org/10.3390/genes9020068
Chicago/Turabian Style
Littink, Karin W., Patricia T. Y. Stappers, Frans C. C. Riemslag, Herman E. Talsma, Maria M. Van Genderen, Frans P. M. Cremers, Rob W. J. Collin, and L. Ingeborgh Van den Born.
2018. "Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome" Genes 9, no. 2: 68.
https://doi.org/10.3390/genes9020068
APA Style
Littink, K. W., Stappers, P. T. Y., Riemslag, F. C. C., Talsma, H. E., Van Genderen, M. M., Cremers, F. P. M., Collin, R. W. J., & Van den Born, L. I.
(2018). Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes, 9(2), 68.
https://doi.org/10.3390/genes9020068