Literature DB >> 8803781

Multiple deletions of mitochondrial DNA in muscle from a patient with benign progressive external ophthalmoplegia.

Y Campos1, M A Martín, J C Rubio, C Ricard, A Cabello, J Arenas.   

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Year:  1996        PMID： 8803781     DOI： 10.1007/bf01799268

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  3 in total

1.  An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.

Authors:  M Zeviani; S Servidei; C Gellera; E Bertini; S DiMauro; S DiDonato
Journal:  Nature       Date:  1989-05-25       Impact factor: 49.962

Review 2.  Mitochondrial encephalomyopathies.

Authors:  S DiMauro; C T Moraes
Journal:  Arch Neurol       Date:  1993-11

3.  Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.

Authors:  Y Campos; T Garcia-Silva; C R Barrionuevo; A Cabello; R Muley; J Arenas
Journal:  Pediatr Neurol       Date:  1995-07       Impact factor: 3.372
  3 in total

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