Literature DB >> 9484389

Myoclonus epilepsy with ragged red fibers and multiple mtDNA deletions.

D T Blumenthal1, S Shanske, S S Schochet, F M Santorelli, S DiMauro, M Jaynesm, J Bodensteiner.   

Abstract

In a patient with clinical features of myoclonus epilepsy with ragged red fibers (MERRF), molecular genetic analysis of mitochondrial DNA did not show either of the two point mutations typically associated with MERRF but did show multiple deletions by Southern blot. This case further illustrates the heterogeneity observed with mtDNA mutations.

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Year:  1998        PMID: 9484389     DOI: 10.1212/wnl.50.2.524

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

1.  A unique junctional palindromic sequence in mitochondrial DNA from a patient with progressive external ophthalmoplegia.

Authors:  T Saiwaki; K Shiga; R Fukuyama; Y Tsutsumi; S Fushiki
Journal:  Mol Pathol       Date:  2000-12

Review 2.  Progressive external ophthalmoplegia characterized by multiple deletions of mitochondrial DNA: unraveling the pathogenesis of human mitochondrial DNA instability and the initiation of a genetic classification.

Authors:  Gert Van Goethem; Jean-Jacques Martin; Christine Van Broeckhoven
Journal:  Neuromolecular Med       Date:  2003       Impact factor: 3.843

3.  Epilepsy in adults with mitochondrial disease: A cohort study.

Authors:  Roger G Whittaker; Helen E Devine; Grainne S Gorman; Andrew M Schaefer; Rita Horvath; Yi Ng; Victoria Nesbitt; Nichola Z Lax; Robert McFarland; Mark O Cunningham; Robert W Taylor; Douglass M Turnbull
Journal:  Ann Neurol       Date:  2015-11-17       Impact factor: 10.422

  3 in total

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