Multiethnic involvement in autosomal-dominant optic atrophy in Singapore
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://www.nature.com/articles/eye2016255.pdf
Reference37 articles.
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3. Delettre C, Lenaers G, Griffoin J-M, Gigarel N, Lorenzo C, Belenguer P et al. Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy. Nat Genet 2000; 26 (2): 207–210.
4. Alexander C, Votruba M, Pesch UEA, Thiselton DL, Mayer S, Moore A et al. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nat Genet 2000; 26 (2): 211–215.
5. Chao de la Barca JM, Prunier-Mirebeau D, Amati-Bonneau P, Ferré M, Sarzi E, Bris C et al. OPA1-related disorders: diversity of clinical expression, modes of inheritance and pathophysiology. Neurobiol Dis 2016; 90: 20–26.
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