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A hereditary spastic paraplegia mutation in kinesin-1A/KIF5A disrupts neurofilament transport

Overview of attention for article published in Molecular Neurodegeneration, November 2010
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Citations

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Title
A hereditary spastic paraplegia mutation in kinesin-1A/KIF5A disrupts neurofilament transport
Published in
Molecular Neurodegeneration, November 2010
DOI 10.1186/1750-1326-5-52
Pubmed ID
Authors

Lina Wang, Anthony Brown

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 56 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 56 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 9 16%
Researcher 8 14%
Student > Doctoral Student 8 14%
Student > Master 6 11%
Student > Postgraduate 4 7%
Other 7 13%
Unknown 14 25%
Readers by discipline Count As %
Agricultural and Biological Sciences 12 21%
Neuroscience 9 16%
Biochemistry, Genetics and Molecular Biology 9 16%
Medicine and Dentistry 6 11%
Physics and Astronomy 2 4%
Other 5 9%
Unknown 13 23%