Literature DB >> 10970191

Further evidence for genetic heterogeneity of autosomal dominant disorders with accumulation of multiple deletions of mitochondrial DNA.

G van Goethem, A Löfgren, J J Martin, C van Broeckhoven.   

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Year:  2000        PMID： 10970191      PMCID： PMC1734637          DOI： 10.1136/jmg.37.7.547

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  2 in total

Review 1.  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

2.  POS5 gene of Saccharomyces cerevisiae encodes a mitochondrial NADH kinase required for stability of mitochondrial DNA.

Authors:  Micheline K Strand; Gregory R Stuart; Matthew J Longley; Maria A Graziewicz; Olivia C Dominick; William C Copeland
Journal:  Eukaryot Cell       Date:  2003-08
  2 in total

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