Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy-Reference-Cited by-同舟云学术

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

Published:1994-05 Issue:1-2 Volume:123 Page:74-79
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

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.

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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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