The role of mitochondria in inherited neurodegenerative diseases
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-4159.2006.03990.x/fullpdf
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1. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
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3. Sequence and organization of the human mitochondrial genome
4. Presenilin-1 is located in rat mitochondria
5. Membrane protein degradation by AAA proteases in mitochondria
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