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FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes

Overview of attention for article published in Behavioral and Brain Functions, June 2011
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33 Mendeley
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Title
FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes
Published in
Behavioral and Brain Functions, June 2011
DOI 10.1186/1744-9081-7-19
Pubmed ID
Authors

Ana I. Seixas, José Vale, Paula Jorge, Isabel Marques, Rosário Santos, Isabel Alonso, Ana M. Fortuna, Jorge Pinto-Basto, Paula Coutinho, Russell L. Margolis, Jorge Sequeiros, Isabel Silveira

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 33 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 33 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 18%
Student > Bachelor 4 12%
Professor 3 9%
Student > Master 3 9%
Student > Ph. D. Student 2 6%
Other 4 12%
Unknown 11 33%
Readers by discipline Count As %
Psychology 5 15%
Medicine and Dentistry 4 12%
Nursing and Health Professions 2 6%
Agricultural and Biological Sciences 2 6%
Biochemistry, Genetics and Molecular Biology 2 6%
Other 5 15%
Unknown 13 39%