1. Mendelian inheritance in man;McKusick, V.A.,1992
2. Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis;Larsson, L.E.; Linderholm, H.; Muller, R.; Ringqvist, T.; Sornas, R.,1964
3. Hereditary abnormal muscle metabolism with hyperkinetic circulation found along the rivers in northern Sweden, often along one single river valley.20 during exercise;Linderholm, H.; Muller, R.; Ringqvist, T.; Sornas, R.;Acta Med Scand
4. Low succinate dehydrogenase (SDH) activity in a patient with a hereditary myopathy with paroxysmal myoglobinuria;Linderholm, H.; Essen-Gustavsson, B.; Thornell, L.E.;J Intern Med,1990
5. Deficiency of skeletal muscle succinate dehydrogenase and aconitase. B has been found. Furthermore, both parents of family A and the father of family I are linked Pathophysiology of exercise in a novel human muscle oxidative defect;Haller, R.G.; Henriksson, K.G.; Jorfeldt, L.;J Clin Invest,1991