Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene
Genetics
.
1993 Jan;133(1):133-6.
doi: 10.1093/genetics/133.1.133.
Authors
N Howell
,
I Kubacka
,
S Halvorson
,
D Mackey
PMID:
8417984
PMCID:
PMC1205293
DOI:
10.1093/genetics/133.1.133
No abstract available
Publication types
Letter
Research Support, U.S. Gov't, P.H.S.
MeSH terms
Cytochrome b Group / genetics*
Female
Humans
Male
Mitochondria / enzymology*
Mutation*
Optic Atrophies, Hereditary / genetics*
Substances
Cytochrome b Group
Grants and funding
P01 HD08315/HD/NICHD NIH HHS/United States