Author:
Nguyen D,Alavi M V,Kim K-Y,Kang T,Scott R T,Noh Y H,Lindsey J D,Wissinger B,Ellisman M H,Weinreb R N,Perkins G A,Ju W-K
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Cell Biology,Cellular and Molecular Neuroscience,Immunology
Reference40 articles.
1. Alexander C, Votruba M, Pesch UE, 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: 211–215.
2. Delettre C, Lenaers G, Griffoin JM, 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: 207–210.
3. Johnston PB, Gaster RN, Smith VC, Tripathi RC . A clinicopathologic study of autosomal dominant optic atrophy. Am J Ophthalmol 1979; 88: 868–875.
4. Kjer P, Jensen OA, Klinken L . Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy. Acta Ophthalmol (Copenh) 1983; 61: 300–312.
5. Alavi MV, Bette S, Schimpf S, Schuettauf F, Schraermeyer U, Wehrl HF et al. A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy. Brain 2007; 130 (Part 4): 1029–1042.
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