Case of phenotype of optic nerve atrophy due to mutation in С19orf12 gene (neurodegeneration with the brain iron accumulation (nbia))

Case of phenotype of optic nerve atrophy due to mutation in С19orf12 gene (neurodegeneration with the brain iron accumulation (nbia))

<p> <b>M.E. Ivanova<sup>1</sup>, V.V. Kadyshev<sup>2</sup>, D.S. Atarshchikov<sup>3</sup>, I.V. Zolnikova<sup>4</sup>, N.P. Akchurina<sup>4</sup>, N.K. Serova<sup>5</sup>, F.A. Konovalov<sup>6</sup>, E.R...

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Bibliographic Details
Main Authors:	M.E. Ivanova, V.V. Kadyshev, D.S. Atarshchikov, I.V. Zolnikova, N.P. Akchurina, N.K. Serova, F.A. Konovalov, E.R. Lozier, E.A. Pomerantseva, N.V. Vetrova, D. Barh, L.M. Balashova, J.M. Salmasi
Format:	Article
Language:	Russian
Published:	Prime-Media 2020-03-01
Series:	РМЖ "Клиническая офтальмология"
Online Access:	http://clinopht.com/upload/iblock/16c/16cd519845b39d8d7a872a0c28bfe338.pdf

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