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October 20, 2005Annals of NeurologyOpen Access

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness

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Authors

PAPatrizia Amati‐BonneauCentre National de la Recherche Scientifique AGAgnès GuichetCentre National de la Recherche Scientifique AOAurélien OlichonInserm

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Cite This Study

Amati‐Bonneau et al. (2005) studied this question.

synapsesocial.com/papers/6a79906014b028facf0dd8d9 https://doi.org/10.1002/ana.20681

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Also Consider

Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context:

1Deficit of in vivo mitochondrial ATP production in OPA1‐related dominant optic atrophy2004 · 140 citations
2OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract2004 · 159 citations