Ning Wang

发表

CRISPR/Cas9-based genome editing for the modification of multiple duplications that cause Duchenne muscular dystrophy

Min-ting Lin, Zhiqiang Wang, Ming Jin, 2022, Gene therapy.

GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy

Wanjin Chen, Min-ting Lin, Longquan Chen, 2022, Annals of neurology.

Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China

Wanjin Chen, Ning Wang, Jin He, 2018, Molecular Neurodegeneration.

Cryptic exon activation causes dystrophinopathy in two Chinese families

Ning Wang, Zhiqiang Wang, Ming Jin, 2020, European Journal of Human Genetics.

Base editing-mediated splicing correction therapy for spinal muscular atrophy

Ning Wang, Erwei Zuo, Wenqin Ying, 2020, Cell Research.

The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy

Min-ting Lin, Longquan Chen, Zhiqiang Wang, 2023, Annals of clinical and translational neurology.

Heterozygous Seryl‐tRNA Synthetase 1 Variants Cause Charcot–Marie–Tooth Disease

M. Kennerson, Jin He, Jing Zhang, 2022, Annals of neurology.

Loss of function of CMPK2 causes mitochondria deficiency and brain calcification

Z. Xiong, Min-ting Lin, C. Liou, 2022, Cell Discovery.

Whole Exome Sequencing Identifies Two Novel Mutations in the Reticulon 4–Interacting Protein 1 Gene in a Chinese Family with Autosomal Recessive Optic Neuropathies

Xin-Xin Guo, Qi-Jie Zhang, Chong Wang, 2019, Journal of Molecular Neuroscience.

Expanding the phenotype and genotype spectra of PLIN4-associated myopathy with rimmed ubiquitin-positive autophagic vacuolation

Min-ting Lin, Longquan Chen, Zhiqiang Wang, 2022, Acta Neuropathologica.

Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

Min-ting Lin, Longquan Chen, Yi Lin, 2023, Neurology.

Atypical features in two adult patients with Cockayne syndrome and analysis of genotype-phenotype correlation.

Ning Wang, Hao-Ling Cheng, Zhi-Ying Wu, 2023, Chinese medical journal.

Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia

Yusen Qiu, Xiang Lin, Yi-Jun Chen, 2023, Movement disorders : official journal of the Movement Disorder Society.

Cerebral-Cerebellar Cortical Activity and Connectivity Underlying Sensory Trick in Cervical Dystonia.

Yurong Li, Ning Wang, Naiqing Cai, 2024, Annals of clinical and translational neurology.

Lacunes are associated with late-stage multiple sclerosis comorbidities

Zaiqiang Zhang, Aiyu Lin, Ying Fu, 2023, Frontiers in neurology.