[Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome]. [electronic resource]
Producer: 20090303Description: 273-8 p. digitalISSN:- 1003-9406
- Adolescent
- Adult
- Blotting, Southern
- Child
- DNA Mutational Analysis
- DNA, Mitochondrial -- chemistry
- Female
- Gene Deletion
- Humans
- Kearns-Sayre Syndrome -- genetics
- Male
- Middle Aged
- Ophthalmoplegia, Chronic Progressive External -- genetics
- Point Mutation
- Polymerase Chain Reaction -- methods
- Polymorphism, Restriction Fragment Length
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Publication Type: English Abstract; Journal Article; Research Support, Non-U.S. Gov't
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