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. |
X Demographics
The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Geographical breakdown
Country | Count | As % |
---|---|---|
United Kingdom | 1 | 100% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 1 | 100% |
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% |