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Hongfu Li

13PUBLICATIONS
3CO-AUTHORS
South-East Asian languages (excl. Indonesian)Neurology and neuromuscular diseasesInfant and child healthCancer geneticsSensory systems
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Journal

Publications (13)

Sort by Publication Date:
|Oct 01, 2024
Clinical characterization and founder effect analysis in Chinese amyotrophic lateral sclerosis patients with <i>SOD1</i> common variants.

Pei-Shan Wang, Xin-Xia Yang, Qiao Wei

|Sep 24, 2024
Blood diagnostic and prognostic biomarkers in amyotrophic lateral sclerosis.

Yongting Lv, Hongfu Li

|Nov 28, 2023
Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype.

Qiao Wei, Hao Yu, Pei-Shan Wang

|Sep 01, 2022
Novel stop-gain RNF170 variation detected in a Chinese family with adolescent-onset hereditary spastic paraplegia.

Jing-Xin Fu, Qiao Wei, Yu-Lan Chen

|May 28, 2022
Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration.

Hao-Ling Cheng, Yi-Jun Chen, Yan-Yan Xue

|Mar 29, 2022
A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia.

Qiao Wei, Pei-Shan Wang, Hai-Lin Dong

Pageof 3

Frequent Collaborators

6 joint publications

Zhi-Ying Wu

1 joint publications

Hai-Lin Dong

1 joint publications

Ning Wang

Frequent Collaborators

6 joint publications

Zhi-Ying Wu

1 joint publications

Hai-Lin Dong

1 joint publications

Ning Wang

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