Hong‐Xia Fu

Spectrum of <i>SLC20A2</i> , <i>PDGFRB</i> , <i>PDGFB</i> , and <i>XPR1</i> mutations in a large cohort of patients with primary familial brain calcification

Xiaohuan Zou, Chong Wang, Xiang‐Ping Yao et al. · Human Mutation · 2019 · 48 citations

Life Sciences, Genetics, Molecular Genetics +17

Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency

Hong‐Xia Fu, Xinyi Liu, Zhiqiang Wang et al. · Neurological Sciences · 2016 · 31 citations

Life Sciences, Genetics, Molecular Genetics +11

Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations

Xin-Yi Liu, Ming Jin, Zhiqiang Wang et al. · Chinese Medical Journal · 2016 · 13 citations · Full text

Medicine, Genetics, Neurology +17