82171403/National Natural Science Foundation of China[Grants and Funding] - Search Results

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Year	Number of Results
2023	1
2024	3

Page 1

Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization.

Lin X, Jiang JY, Hong DJ, Lin KJ, Li JJ, Chen YJ, Qiu YS, Wang Z, Liao YC, Yang K, Shi Y, Wang MW, Hsu SL, Hong S, Zeng YH, Chen XC, Wang N, Lee YC, Chen WJ. Lin X, et al. Mov Disord. 2024 Jan;39(1):152-163. doi: 10.1002/mds.29664. Epub 2023 Nov 28. Mov Disord. 2024. PMID: 38014483

A Homoplasmic MT-TV Mutation Associated with Mitochondrial Inheritance of Hereditary Spastic Paraplegia.

Shi Y, Xie J, Jiang J, Yan X, Chen X, Hong S, Liu J, Xu G, Su H, Chen W, Wang N, Lin X. Shi Y, et al. Mov Disord. 2024 Oct 28. doi: 10.1002/mds.30048. Online ahead of print. Mov Disord. 2024. PMID: 39468830

A pseudo-homozygous missense variant and Alu-mediated exon 5 deletion in FARS2 causing spastic paraplegia 77.

Lin SH, Xie JH, Jiang JY, Yan XY, Hong CY, Chen WJ, Wang N, Lin X. Lin SH, et al. Ann Clin Transl Neurol. 2024 Nov;11(11):3019-3024. doi: 10.1002/acn3.52195. Epub 2024 Sep 28. Ann Clin Transl Neurol. 2024. PMID: 39342436 Free PMC article.

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