mtDNA Mutations That Cause Optic Neuropathy: How Do We Know?

Author:

Howell Neil,Bogolin Christy,Jamieson Robyn,Marenda Daniel R.,Mackey David A.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference31 articles.

1. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981

2. Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1);Brown;Arch Ophthalmol,1997

3. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations;Brown;Hum Mutat,1995

4. Spectrum of mitochondrial DNA mutations in Leber's hereditary optic neuropathy;Brown;Clin Neurosci,1994

5. Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia;De Vries;Am J Hum Genet,1996

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