Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy. [electronic resource]
Producer: 19901109Description: 1417-20 p. digitalISSN:- 0003-9950
- Adult
- Base Sequence
- DNA, Mitochondrial -- genetics
- Deoxyribonucleases, Type II Site-Specific
- Electrophoresis, Polyacrylamide Gel
- Humans
- Male
- Molecular Sequence Data
- Mutation
- Optic Atrophies, Hereditary -- diagnosis
- Pedigree
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- Visual Acuity
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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