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Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan

Overview of attention for article published in Orphanet Journal of Rare Diseases, August 2017
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Title
Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan
Published in
Orphanet Journal of Rare Diseases, August 2017
DOI 10.1186/s13023-017-0703-4
Pubmed ID
Authors

Mariko Okubo, Kanako Goto, Hirofumi Komaki, Harumasa Nakamura, Madoka Mori-Yoshimura, Yukiko K. Hayashi, Satomi Mitsuhashi, Satoru Noguchi, En Kimura, Ichizo Nishino

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 41 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 41 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 7 17%
Other 5 12%
Researcher 5 12%
Student > Master 5 12%
Student > Ph. D. Student 4 10%
Other 6 15%
Unknown 9 22%
Readers by discipline Count As %
Medicine and Dentistry 9 22%
Biochemistry, Genetics and Molecular Biology 8 20%
Neuroscience 3 7%
Pharmacology, Toxicology and Pharmaceutical Science 2 5%
Agricultural and Biological Sciences 2 5%
Other 4 10%
Unknown 13 32%