Open AccessLeber’s Hereditary Optic Neuropathy Plus Causing Recurrent Myelopathy due to an MT-DN1 Mutation at G3635A
Author(s) -
Elijah Lackey,
Ariel Lefland,
Christopher Eckstein
Publication year - 2022
Publication title -
case reports in neurological medicine
Language(s) - English
Resource type - Journals
eISSN - 2090-6668
pISSN - 2090-6676
DOI - 10.1155/2022/1628892
Subject(s) - medicine , leber's hereditary optic neuropathy , mutation , optic neuropathy , myelopathy , dermatology , pediatrics , genetics , ophthalmology , optic nerve , gene , psychiatry , spinal cord , biology
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