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Hong-xia Fu
Hong-xia Fu
Fujian Medical University
Medicine
gene mutation
Multiple Acyl-CoA Dehydrogenase Deficiency
Posterior compartment of thigh
Muscle biopsy
3
Papers
31
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CHIP control degradation of mutant ETF:QO through ubiquitylation in late-onset multiple acyl-CoA dehydrogenase deficiency.
2021
Journal of Inherited Metabolic Disease
Xin-Yi Liu
Xue-Jiao Chen
Miao Zhao
Zhiqiang Wang
Hai-Zhu Chen
Hong-Fu Li
Chen-Ji Wang
Shi-Fei Wu
Chao Peng
Yue Yin
Hong-xia Fu
Min-Ting Lin
Long Yu
Zhi-Qi Xiong
Zhi-Ying Wu
Ning Wang
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Citations (1)
Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency
2016
Neurological Sciences
Hong-xia Fu
Xin-Yi Liu
Zhi-Qiang Wang
Ming Jin
Dan-Ni Wang
Jun-Jie He
Min-Ting Lin
Ning Wang
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Citations (20)
Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations
2016
Chinese Medical Journal
Xin-Yi Liu
Ming Jin
Zhi-Qiang Wang
Dan-Ni Wang
Jun-Jie He
Min-Ting Lin
Hong-xia Fu
Ning Wang
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Citations (10)
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