Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy
- 30 September 2006
- journal article
- research article
- Published by Elsevier BV in Experimental Eye Research
- Vol. 83 (3), 702-706
- https://doi.org/10.1016/j.exer.2006.03.004
Abstract
No abstract availableKeywords
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