High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy.

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OPA1 analysis in an international series of probands with bilateral optic atrophy.

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High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy.

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High frequency of OPA1 mutatio ...... n south-eastern Sicily, Italy.

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High frequency of OPA1 mutatio ...... n south-eastern Sicily, Italy.

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High frequency of OPA1 mutatio ...... n south-eastern Sicily, Italy.

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High frequency of OPA1 mutatio ...... n south-eastern Sicily, Italy.

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High frequency of OPA1 mutatio ...... n south-eastern Sicily, Italy.

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High frequency of OPA1 mutatio ...... n south-eastern Sicily, Italy.

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High frequency of OPA1 mutatio ...... in south-eastern Sicily, Italy

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P2860

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

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OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

USH1A: chronicle of a slow death

Haploview: analysis and visualization of LD and haplotype maps

Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy

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

Mitochondrial dysfunction as a cause of optic neuropathies

Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12.

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277-282

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scholarly article

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10.1111/J.1399-0004.2011.01751.X

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Antonio Federico

Gian Nicola Gallus

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2011-08-15T00:00:00Z

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21745197

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An Eadailt

High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy.

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P2860

P2860

High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy.

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