Project Details
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Analyse der molekulargenetischen und biochemischen Heterogenität im Skelettmuskel von Patienten mit mitochondrialen Zytopathien

Applicant Professor Dr. Wolfram S. Kunz, since 1/2006
Subject Area Molecular Biology and Physiology of Neurons and Glial Cells
Term from 2003 to 2008
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 5412408
 
Final Report Year 2008

Final Report Abstract

No abstract available

Publications

  • Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosis. Graefes Arch Clin Exp Ophthalmol. 2005;243(4):380-2
    Okulla T, Kunz WS, Klockgether T, Schröder R, Kornblum C
  • Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy. Nat Genet. 2005;37(8):873-7
    Zsurka G, Kraytsberg Y, Kudina T, Kornblum C, Elger CE, Khrapko K, Kunz WS
  • Inheritance of mitochondrial DNA recombinants in double-heteroplasmic families: potential implications for phylogenetic analysis. Am J Hum Genet. 2007;80(2):298-305
    Zsurka G, Hampel KG, Kudina T, Kornblum C, Kraytsberg Y, Elger CE, Khrapko K, Kunz WS
 
 

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