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Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency associated with two novel mutations: a case report
BMC Pediatrics, October 2019
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
The data shown below were compiled from readership statistics for 22 Mendeley readers of this research output. Click here to see the associated Mendeley record.
|Readers by professional status||Count||As %|
|Student > Postgraduate||2||9%|
|Student > Doctoral Student||1||5%|
|Student > Bachelor||1||5%|
|Readers by discipline||Count||As %|
|Medicine and Dentistry||4||18%|
|Nursing and Health Professions||3||14%|
|Biochemistry, Genetics and Molecular Biology||1||5%|
|Immunology and Microbiology||1||5%|
|Arts and Humanities||1||5%|