Novel biallelic compound heterozygous mutations in FDXR cause optic atrophy in a young female patient: a case report

doi:10.18240/ijo.2021.11.22

Home > Archive>Volume 14, Issue 11, 2021 >1796-1798. DOI:10.18240/ijo.2021.11.22

Novel biallelic compound heterozygous mutations in FDXR cause optic atrophy in a young female patient: a case report
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                        10.18240/ijo.2021.11.22
                    
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Corresponding Author:Ying Hong. Department of Ophthalmology, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing 100191, China. drhongying@bjmu.edu.cn
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Fund Project:Supported by National Natural Science Foundation of China (No.81970798; No.81670851).

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Si-Jia Song, Ying Hong, Ke Xu, et al. Novel biallelic compound heterozygous mutations in FDXR cause optic atrophy in a young female patient: a case report. Int J Ophthalmol, 2021,14(11):1796-1798

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Publication History

Received:December 28,2020
Revised:March 03,2021
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Online: October 27,2021
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