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Clinical Features of Chinese Sporadic Leber Hereditary Optic Neuropathy Caused by Rare Primary mtDNA Mutations

Cui, SL; Yang, L; Jiang, HQ; Peng, JT; Shang, J; Wang, JW; Zhang, XJ

Cui, SL (corresponding author), Capital Med Univ, Beijing Tongren Hosp, Dept Neurol, 1 Dongjiaominxiang St, Beijing 100730, Peoples R China.

JOURNAL OF NEURO-OPHTHALMOLOGY, 2020; 40 (1): 30

Abstract

Objective: The primary aim of this study was to describe clinical features of Chinese sporadic Leber hereditary optic neuropathy (LHON) caused by rare......

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