Article Versions Notes

Roosing S, Cremers FPM, Riemslag FCC, Zonneveld-Vrieling MN, Talsma HE, Klessens-Godfroy FJM, Den Hollander AI, Van den Born LI. A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290. Genes. 2017; 8(8):208. https://doi.org/10.3390/genes8080208

Roosing, Susanne, Frans P. M. Cremers, Frans C. C. Riemslag, Marijke N. Zonneveld-Vrieling, Herman E. Talsma, Francoise J. M. Klessens-Godfroy, Anneke I. Den Hollander, and L. Ingeborgh Van den Born. 2017. "A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290" Genes 8, no. 8: 208. https://doi.org/10.3390/genes8080208

Roosing, S., Cremers, F. P. M., Riemslag, F. C. C., Zonneveld-Vrieling, M. N., Talsma, H. E., Klessens-Godfroy, F. J. M., Den Hollander, A. I., & Van den Born, L. I. (2017). A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290. Genes, 8(8), 208. https://doi.org/10.3390/genes8080208