Novel biallelic compound heterozygous mutations in FDXR cause optic atrophy in a young female patient: a case report
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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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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
  • Adopted:
  • Online: October 27,2021
  • Published: