A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy. (Q42950908)
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scientific article published on May 1995
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy. |
scientific article published on May 1995 |
Statements
A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy (English)
T Lamminen
A Majander
V Juvonen
M Wikström
P Aula
E Nikoskelainen
M L Savontous
1 reference