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Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy

Overview of attention for article published in BMC Medical Genomics, September 2013
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Title
Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy
Published in
BMC Medical Genomics, September 2013
DOI 10.1186/1471-2350-14-89
Pubmed ID
Authors

Anna Ardissone, Cinzia Bragato, Lorella Caffi, Flavia Blasevich, Sabrina Maestrini, Maria Luisa Bianchi, Lucia Morandi, Isabella Moroni, Marina Mora

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 49 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Japan 1 2%
Unknown 48 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 11 22%
Researcher 10 20%
Student > Doctoral Student 4 8%
Student > Master 4 8%
Other 3 6%
Other 9 18%
Unknown 8 16%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 15 31%
Medicine and Dentistry 7 14%
Agricultural and Biological Sciences 7 14%
Nursing and Health Professions 2 4%
Neuroscience 2 4%
Other 5 10%
Unknown 11 22%