Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations

J Med Genet. 1995 Feb;32(2):81-7. doi: 10.1136/jmg.32.2.81.

Authors

P Riordan-Eva¹, A E Harding

Affiliation

¹ Department of Neuro-Ophthalmology, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.

No abstract available

Publication types

Review

MeSH terms

DNA, Mitochondrial / genetics*
Female
Fundus Oculi
Genetic Counseling
Heart Diseases / genetics
Humans
Male
Nervous System Diseases / genetics
Optic Atrophies, Hereditary / genetics*
Optic Atrophies, Hereditary / physiopathology*
Point Mutation / genetics
Prognosis
Vision, Ocular

Substances

DNA, Mitochondrial