175th ENMC International Workshop: Mitochondrial protein synthesis in health and disease, 25–27th June 2010, Naarden, The Netherlands
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference33 articles.
1. Mitochondrial DNA mutations in human disease;Taylor;Nat Rev Genet,2005
2. Inherited mitochondrial diseases of DNA replication;Copeland;Annu Rev Med,2008
3. Structure of the mammalian mitochondrial ribosome reveals an expanded functional role for its component proteins;Sharma;Cell,2003
4. Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation;Miller;Ann Neurol,2004
5. Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation;Saada;J Med Genet,2007
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