Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qter (original) (raw)
Clinical Features, Molecular Genetics, and Pathophysiology of Dominant Optic Atrophy.
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Journal of medical genetics, 1998
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Genetic Refinement of Dominant Optic Atrophy (OPA1) Locus to Within a 2 CM Interval of Chromosome 3q.
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Subclinical multisystem neurologic disease in "pure" OPA1 autosomal dominant optic atrophy
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The Pattern of Retinal Ganglion Cell Loss in OPA1-Related Autosomal Dominant Optic Atrophy Inferred From Temporal, Spatial, and Chromatic Sensitivity Losses
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Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type Kjer
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Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy
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