A wide variety of reflective gear running options are available to you, such as free samples, paid samples. Sciare Comprensorio sciistico Nassfeld Pramollo. Boost your performance on longer hikes with this quick-drying, long-sleeve tee that has a shaped hem for subtle style and extra coverage. The region has been declared Nature Park of
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Biochemical and ultrastructural studies of mitochondria in Luft's disease: Trans Am Neurol Assoc ; Muscle carnitine palmityltransferase deficiency and myoglobinuria. A disorder of muscle lipid metabolism and myoglobinuria. New Engl J Med ; Fatal infantile form of muscle phosphorylase deficiency. Neuromuscular disorder in five adults. Ann Neurol ; 5: Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome c oxidase deficiency.
A distinct form of adult polyglucosan body disease with massive involvement of central and peripheral neuronal processes and astrocytes. Human muscle phosphoglycerate mutase deficiency: A newly discovered metabolic myopathy. Phosphoglycerate kinase PGK deficiency: Another cause of recurrent myoglobinuria.
Ann Neurol ; Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: A distinctive clinical syndrome.
Cytochrome c oxidase deficiency in Leigh syndrome. A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
Mitochondrial DNA depletion with variable tissue expression: Am J Hum Genet ; Molecular genetic heterogeneity of myophosphorylase deficiency McArdle's disease. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA. New Engl J Med ; Familial cerebellar ataxia with muscle coenzyme Q10 deficiency. Deficiency of tetralinoleyl-cardiolipin in Barth syndrome. Cerebellar ataxia and coenzyme Q10 deficiency.
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