MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathy.
Document type:
Zeitschriftenaufsatz
Author(s):
Becker, L. ; Kling, E. ; Schiller, E. ; Zeh, R. ; Schrewe, A. ; Hölter, S.M. ; Mossbrugger, I. ; Calzada-Wack, J.C. ; Strecker, V. ; Wittig, I. ; Dumitru, I. ; Wenz, T. ; Bender, A. ; Aichler, M. ; Janik, D. ; Neff, F. ; Walch, A.K. ; Quintanilla-Fend, L. ; Floß, T. ; Bekeredjian, R. ; Gailus-Durner, V. ; Fuchs, H. ; Wurst, W. ; Meitinger, T. ; Prokisch, H. ; Hrabé de Angelis, M. ; Klopstock, T.
Keywords:
Genetics and Epidemiology ; Enabling and Novel Technologies
Research Programmes: Genes and Environment in Common Diseases ; Research Units: Research Unit Analytical Pathology (AAP)
TUM Institution:
Institute of Experimental Genetics (IEG) ; Institute of Developmental Genetics (IDG) ; Institute of Pathology (PATH) ; Institute of Human Genetics (IHG)