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A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family

Overview of attention for article published in BMC Medical Genomics, March 2019
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Title
A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family
Published in
BMC Medical Genomics, March 2019
DOI 10.1186/s12881-019-0781-3
Pubmed ID
Authors

Ningjin Wu, Husile Husile, Liqing Yang, Yaning Cao, Xing Li, Wenyan Huo, Haihua Bai, Yangjian Liu, Qizhu Wu

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 12 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 12 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 17%
Student > Doctoral Student 2 17%
Professor > Associate Professor 1 8%
Student > Postgraduate 1 8%
Unknown 6 50%
Readers by discipline Count As %
Medicine and Dentistry 2 17%
Biochemistry, Genetics and Molecular Biology 1 8%
Sports and Recreations 1 8%
Nursing and Health Professions 1 8%
Unknown 7 58%