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Dystrophin Gene Mutation Location and the Risk of Cognitive Impairment in Duchenne Muscular Dystrophy

Overview of attention for article published in PLOS ONE, January 2010
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Title
Dystrophin Gene Mutation Location and the Risk of Cognitive Impairment in Duchenne Muscular Dystrophy
Published in
PLOS ONE, January 2010
DOI 10.1371/journal.pone.0008803
Pubmed ID
Authors

Peter J. Taylor, Grant A. Betts, Sarah Maroulis, Christian Gilissen, Robyn L. Pedersen, David R. Mowat, Heather M. Johnston, Michael F. Buckley

Abstract

A significant component of the variation in cognitive disability that is observed in Duchenne muscular dystrophy (DMD) is known to be under genetic regulation. In this study we report correlations between standardised measures of intelligence and mutational class, mutation size, mutation location and the involvement of dystrophin isoforms.

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Mendeley readers

The data shown below were compiled from readership statistics for 191 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Brazil 3 2%
Netherlands 2 1%
Colombia 1 <1%
Italy 1 <1%
Germany 1 <1%
Tunisia 1 <1%
Spain 1 <1%
Unknown 181 95%

Demographic breakdown

Readers by professional status Count As %
Student > Master 30 16%
Student > Bachelor 30 16%
Researcher 28 15%
Student > Ph. D. Student 26 14%
Professor 8 4%
Other 30 16%
Unknown 39 20%
Readers by discipline Count As %
Medicine and Dentistry 40 21%
Agricultural and Biological Sciences 36 19%
Biochemistry, Genetics and Molecular Biology 22 12%
Neuroscience 12 6%
Psychology 12 6%
Other 22 12%
Unknown 47 25%