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Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes

Overview of attention for article published in PLOS ONE, December 2010
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Title
Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
Published in
PLOS ONE, December 2010
DOI 10.1371/journal.pone.0015687
Pubmed ID
Authors

Bekim Sadikovic, Jing Wang, Ayman El-Hattab, Megan Landsverk, Ganka Douglas, Ellen K. Brundage, William J. Craigen, Eric S. Schmitt, Lee-Jun C. Wong

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 63 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Portugal 1 2%
Ireland 1 2%
Brazil 1 2%
Russia 1 2%
United States 1 2%
Unknown 58 92%

Demographic breakdown

Readers by professional status Count As %
Researcher 14 22%
Student > Ph. D. Student 9 14%
Student > Bachelor 8 13%
Student > Master 5 8%
Professor > Associate Professor 4 6%
Other 12 19%
Unknown 11 17%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 17 27%
Agricultural and Biological Sciences 13 21%
Medicine and Dentistry 11 17%
Neuroscience 3 5%
Business, Management and Accounting 2 3%
Other 5 8%
Unknown 12 19%