Retinal abnormalities associated with a mutation of the nucleotide 683 in von Hippel-Lindau disease.

MLA

Piermarocchi, S., et al. “Retinal Abnormalities Associated with a Mutation of the Nucleotide 683 in von Hippel-Lindau Disease.” Graefe’s Archive for Clinical and Experimental Ophthalmology = Albrecht von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie, vol. 238, no. 7, July 2000, pp. 615–20. EBSCOhost, https://doi.org/10.1007/s004170000129.

APA

Piermarocchi, S., Lo Giudice, G., Pilotto, E., Bertoja, E., Scaroni, C., Martella, M., Opocher, G., & Murgia, A. (2000). Retinal abnormalities associated with a mutation of the nucleotide 683 in von Hippel-Lindau disease. Graefe’s Archive for Clinical and Experimental Ophthalmology = Albrecht von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie, 238(7), 615–620. https://doi.org/10.1007/s004170000129

Chicago

Piermarocchi, S, G Lo Giudice, E Pilotto, E Bertoja, C Scaroni, M Martella, G Opocher, and A Murgia. 2000. “Retinal Abnormalities Associated with a Mutation of the Nucleotide 683 in von Hippel-Lindau Disease.” Graefe’s Archive for Clinical and Experimental Ophthalmology = Albrecht von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie 238 (7): 615–20. doi:10.1007/s004170000129.