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Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports

Overview of attention for article published in BMC Medical Genomics, April 2020
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Title
Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports
Published in
BMC Medical Genomics, April 2020
DOI 10.1186/s12881-020-01010-4
Pubmed ID
Authors

Xiaomei Luo, Jiacheng Hu, Xueren Gao, Yanjie Fan, Yu Sun, Xuefan Gu, Wenjuan Qiu

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 16 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 16 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 25%
Student > Bachelor 4 25%
Researcher 1 6%
Other 1 6%
Unknown 6 38%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 13%
Medicine and Dentistry 2 13%
Agricultural and Biological Sciences 2 13%
Nursing and Health Professions 1 6%
Physics and Astronomy 1 6%
Other 1 6%
Unknown 7 44%