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Identification of a novel SDHB c.563 T > C mutation responsible for Paraganglioma syndrome and genetic analysis of the SDHB gene in China: a case report

Overview of attention for article published in BMC Medical Genomics, May 2020
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Title
Identification of a novel SDHB c.563 T > C mutation responsible for Paraganglioma syndrome and genetic analysis of the SDHB gene in China: a case report
Published in
BMC Medical Genomics, May 2020
DOI 10.1186/s12881-020-01049-3
Pubmed ID
Authors

Heye Chen, Wei Yao, Qing He, Xuefang Yu, Bo Bian

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 2 20%
Student > Ph. D. Student 1 10%
Student > Doctoral Student 1 10%
Student > Master 1 10%
Unknown 5 50%
Readers by discipline Count As %
Medicine and Dentistry 5 50%
Unknown 5 50%