Mitochondrial abnormalities drive cell death in Wolfram syndrome 2
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology
Link
http://www.nature.com/articles/cr200994.pdf
Reference10 articles.
1. Barrett TG, Bundey SE . Wolfram (DIDMOAD) syndrome. J Med Genet 1997; 34:838–841.
2. Amr S, Heisey C, Zhang M, et al. A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible for Wolfram syndrome 2. Am J Hum Genet 2007; 81:673–683.
3. Inoue H, Tanizawa Y, Wasson J, et al. A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome). Nat Genet 1998; 20:143–148.
4. Strom TM, Hortnagel K, Hofmann S, et al. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein. Hum Mol Genet 1998; 7:2021–2028.
5. Bundey S, Poulton K, Whitwell H, Curtis E, Brown IA, Fielder AR . Mitochondrial abnormalities in the DIDMOAD syndrome. J Inherit Metab Dis 1992; 15:315–319.
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