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The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2020
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Title
The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease
Published in
Orphanet Journal of Rare Diseases, January 2020
DOI 10.1186/s13023-019-1291-2
Pubmed ID
Authors

Jorge A. Bevilacqua, Maria del Rosario Guecaimburu Ehuletche, Abayuba Perna, Alberto Dubrovsky, Marcondes C. Franca, Steven Vargas, Madhuri Hegde, Kristl G. Claeys, Volker Straub, Nadia Daba, Roberta Faria, Magali Periquet, Susan Sparks, Nathan Thibault, Roberto Araujo

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 %
Researcher 5 9%
Other 5 9%
Student > Doctoral Student 5 9%
Unspecified 3 5%
Professor 3 5%
Other 7 13%
Unknown 28 50%
Readers by discipline Count As %
Medicine and Dentistry 6 11%
Neuroscience 4 7%
Unspecified 3 5%
Biochemistry, Genetics and Molecular Biology 3 5%
Nursing and Health Professions 3 5%
Other 7 13%
Unknown 30 54%