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Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype

Overview of attention for article published in BMC Neurology, September 2018
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Title
Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype
Published in
BMC Neurology, September 2018
DOI 10.1186/s12883-018-1159-4
Pubmed ID
Authors

Mikko Kärppä, Laura Kytövuori, Markku Saari, Kari Majamaa

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 13 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 15%
Lecturer 1 8%
Student > Bachelor 1 8%
Student > Doctoral Student 1 8%
Student > Ph. D. Student 1 8%
Other 1 8%
Unknown 6 46%
Readers by discipline Count As %
Medicine and Dentistry 4 31%
Agricultural and Biological Sciences 1 8%
Neuroscience 1 8%
Sports and Recreations 1 8%
Unknown 6 46%