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A case report of an intermediate phenotype between congenital myasthenic syndrome and D-2- and L-2-hydroxyglutaric aciduria due to novel SLC25A1 variants

Overview of attention for article published in BMC Neurology, July 2020
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Title
A case report of an intermediate phenotype between congenital myasthenic syndrome and D-2- and L-2-hydroxyglutaric aciduria due to novel SLC25A1 variants
Published in
BMC Neurology, July 2020
DOI 10.1186/s12883-020-01854-6
Pubmed ID
Authors

Wenhui Li, Min Zhang, Linmei Zhang, Yiyun Shi, Lei Zhao, Bingbing Wu, Xihua Li, Shuizhen Zhou

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 27%
Researcher 2 18%
Professor > Associate Professor 2 18%
Student > Master 1 9%
Student > Bachelor 1 9%
Other 1 9%
Unknown 1 9%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 18%
Nursing and Health Professions 2 18%
Medicine and Dentistry 2 18%
Agricultural and Biological Sciences 1 9%
Chemistry 1 9%
Other 1 9%
Unknown 2 18%