Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings
Am J Hum Genet
.
1995 Oct;57(4):954-7.
Authors
R J Oostra
,
C Van den Bogert
,
L G Nijtmans
,
M J van Galen
,
R Zwart
,
P A Bolhuis
,
E M Bleeker-Wagemakers
PMID:
7573056
PMCID:
PMC1801504
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
MeSH terms
Adolescent
Adult
DNA, Mitochondrial / analysis*
Humans
Middle Aged
Optic Atrophies, Hereditary / genetics*
Point Mutation*
Substances
DNA, Mitochondrial