Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy

Author:

Checcarelli Nicoletta,Prelle Allessandro,Moggio Maurizio,Comi Giacomo,Bresolin Nereo,Papadimitriou Alex,Fagiolari Gigliola,Bordoni Andreina,Scarlato Guglielmo

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference25 articles.

1. Progressive cytochrome c oxidase deficiency in a case of Kearns Sayre syndrome: morphological, immunological and biochemical studies in muscle biopsies and autoptic tissues;Bresolin;Ann. Neurol.,1987

2. Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy;Cormier;Am. J. Hum. Genet.,1991

3. Detection of a specific mitochondrial DNA deletion in tissues of older humans;Cortopassi;Nucleic Acid Res.,1990

4. Muscle Biopsy: a practical approach;Dubowitz,1985

5. Autophagic glycogenesis of late onset with mitochondrial abnormalities: light and electron micro-scopic observation;Engel,1968

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