Ivanova, M., Kadyshev, V., Atarshchikov, D., Zolnikova, I., Akchurina, N., Serova, N., . . . Salmasi, J. Case of phenotype of optic nerve atrophy due to mutation in С19orf12 gene (neurodegeneration with the brain iron accumulation (nbia)). Prime-Media.
Chicago Style (17th ed.) CitationIvanova, M.E, et al. Case of Phenotype of Optic Nerve Atrophy Due to Mutation in С19orf12 Gene (neurodegeneration with the Brain Iron Accumulation (nbia)). Prime-Media.
MLA (9th ed.) CitationIvanova, M.E, et al. Case of Phenotype of Optic Nerve Atrophy Due to Mutation in С19orf12 Gene (neurodegeneration with the Brain Iron Accumulation (nbia)). Prime-Media.
Warning: These citations may not always be 100% accurate.