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Journal of Inherited Metabolic Disease|July 9, 2008
Molecular diagnosis of German patients with late-onset glycogen storage disease type IIP R Joshi, D Gläser, S Schmidt, et al.Acta Neurologica Scandinavica|November 17, 2017
Polyglucosan myopathy and functional characterization of a novel GYG1 mutationC Hedberg-Oldfors, A Mensch, K Visuttijai, et al.British Poultry Science|August 26, 2004
Mitochondrial function in turkey skeletal muscle--impact on meat qualityJ R Opalka, M Wicke, F N Gellerich, et al.Neurology|August 10, 2005
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndromeJ S Müller, R Stucka, S Neudecker, et al.Molecular Genetics and Metabolism|March 3, 2006
Molecular and biochemical investigations in fumarase deficiencyM Deschauer, Z Gizatullina, A Schulze, et al.FEBS Letters|July 29, 1991
Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNA(Leu(UUR))]B Obermaier-Kusser, I Paetzke-Brunner, C Enter, et al.Shock (Augusta, Ga.)|June 3, 1999
Impaired energy metabolism in hearts of septic baboons: diminished activities of Complex I and Complex II of the mitochondrial respiratory chainF N Gellerich, S Trumbeckaite, K Hertel, et al.The Journal of Thoracic and Cardiovascular Surgery|June 1, 2001
Doppler microembolic signals in patients with two different types of bileaflet valvesD Georgiadis, S Braun, F Uhlmann, et al.Journal of Neurology|June 21, 2006
Cardiac involvement in limb-girdle muscular dystrophy 2I : conventional cardiac diagnostic and cardiovascular magnetic resonanceC Gaul, M Deschauer, C Tempelmann, et al.Human Genetics|December 1, 1991
A specific point mutation in the mitochondrial genome of Caucasians with MELASC Enter, J Müller-Höcker, S Zierz, et al.Pageof 19