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Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report

Overview of attention for article published in BMC Medical Genomics, November 2020
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Title
Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report
Published in
BMC Medical Genomics, November 2020
DOI 10.1186/s12881-020-01157-0
Pubmed ID
Authors

Yan Wang, Yuhan Chen, San Mei Wang, Xin Liu, Ya Nan Gu, Zhichun Feng

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 14 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 14 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 5 36%
Student > Bachelor 2 14%
Professor 1 7%
Researcher 1 7%
Student > Postgraduate 1 7%
Other 0 0%
Unknown 4 29%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 29%
Medicine and Dentistry 2 14%
Nursing and Health Professions 1 7%
Psychology 1 7%
Neuroscience 1 7%
Other 0 0%
Unknown 5 36%