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1. Biochemische Charakterisierung von Histon-Methyltransferasen aus Drosophila melanogaster


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2. Physical and functional association of SU(VAR)3-9 and HDAC1 in Drosophila

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1084088
http://www.ncbi.nlm.nih.gov/pubmed/11571273  
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3. OPA1 mutations induce mtDNA proliferation in leukocytes of patients with dominant optic atrophy

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525295
http://www.ncbi.nlm.nih.gov/pubmed/22993284  
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4. The Prevalence and Natural History of Dominant Optic Atrophy due to OPA1 Mutations

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC
http://www.ncbi.nlm.nih.gov/pubmed/20417570  
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5. NDUFS8-related Complex I Deficiency Extends Phenotype from “PEO Plus” to Leigh Syndrome

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3755572
http://www.ncbi.nlm.nih.gov/pubmed/23430795  
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6. Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707321
http://www.ncbi.nlm.nih.gov/pubmed/21169334  
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7. Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency


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8. Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency


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9. Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3


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10. Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3


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