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Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency associated with two novel mutations: a case report

Overview of attention for article published in BMC Pediatrics, October 2019
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Title
Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency associated with two novel mutations: a case report
Published in
BMC Pediatrics, October 2019
DOI 10.1186/s12887-019-1747-5
Pubmed ID
Authors

Hao Liu, Jing-kun Miao, Chao-wen Yu, Ke-xing Wan, Juan Zhang, Zhao-jian Yuan, Jing Yang, Dong-juan Wang, Yan Zeng, Lin Zou

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 24 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 24 100%

Demographic breakdown

Readers by professional status Count As %
Other 4 17%
Unspecified 2 8%
Researcher 2 8%
Student > Postgraduate 2 8%
Student > Doctoral Student 1 4%
Other 5 21%
Unknown 8 33%
Readers by discipline Count As %
Medicine and Dentistry 4 17%
Nursing and Health Professions 3 13%
Unspecified 2 8%
Biochemistry, Genetics and Molecular Biology 1 4%
Immunology and Microbiology 1 4%
Other 1 4%
Unknown 12 50%