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A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect.
- Published in:
- Human Genetics, 2001, v. 109, n. 5, p. 498, doi. 10.1007/s004390100600
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- Article
PROCEEDINGS OF THE DANISH OPHTHALMOLOGICAL SOCIETY 1962-1963.
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- Acta Ophthalmologica (1755375X), 1964, v. 42, n. 4, p. 911, doi. 10.1111/j.1755-3768.1964.tb01747.x
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- Article
STUDIES ON AN EPIDEMIC OF KERATOCONJUNCTIVITIS CAUSED BY ADENOVIRUS TYPE 8.
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- Acta Ophthalmologica (1755375X), 1961, v. 39, n. 6, p. 974, doi. 10.1111/j.1755-3768.1961.tb03517.x
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- Article
Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies.
- Published in:
- Brain: A Journal of Neurology, 2010, v. 133, n. 8, p. 2426, doi. 10.1093/brain/awq155
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- Article
Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis.
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- Human Molecular Genetics, 1994, v. 3, n. 6, p. 977
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- Article