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Proceedings of the National Academy of Sciences of the United States of America|January 31, 1995
Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathyA M Moudy, S D Handran, M P Goldberg, et al.
Pediatric Research|May 1, 1996
Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutationF M Santorelli, S C Mak, M E Vazquez-Memije, et al.
Annals of Neurology|October 18, 2001
Autosomal dominant glut-1 deficiency syndrome and familial epilepsyK Brockmann, D Wang, C G Korenke, et al.
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