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A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate

Overview of attention for article published in Genetics and Molecular Biology, January 2021
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Title
A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate
Published in
Genetics and Molecular Biology, January 2021
DOI 10.1590/1678-4685-gmb-2020-0334
Pubmed ID
Authors

Caixia Xian, Mingwei Zhu, Tianying Nong, Yiqiang Li, Xingmei Xie, Xia Li, Jiangui Li, Jingchun Li, Jianping Wu, Weizhe Shi, Ping Wei, Hongwen Xu, Ya-ping Tang

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Mendeley readers

The data shown below were compiled from readership statistics for 1 Mendeley reader of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 1 100%

Demographic breakdown

Readers by professional status Count As %
Professor > Associate Professor 1 100%
Readers by discipline Count As %
Medicine and Dentistry 1 100%