Case reportMitochondrial myopathy and cardiomyopathy in siblings☆
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Cited by (20)
Hypotonia and Weakness: Level of the Muscle
2018, Volpe's Neurology of the NewbornMitochondrial encoded NADH dehydrogenase 5 (MT-ND5) gene point mutation presents as late onset cardiomyopathy
2013, International Journal of CardiologyMitochondrial disorders of the nervous system: Clinical, biochemical, and molecular genetic features
2002, International Review of NeurobiologyAutomatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy
1994, BBA - Molecular Basis of DiseaseInfantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency
1993, Neuromuscular DisordersMitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes
1991, The Journal of Pediatrics
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This study was supported by grants 03X-585 (EH) and 07122 (AO) from the Swedish Medical Research Council, also a grant from Barnhusfonden GbgL 174/87 (EH), First of May Flower Annual Campaign for Children's Health (AO), and the Folke Bernadotte Foundation (MT).
Copyright © 1989 Published by Elsevier Inc.