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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 23, 2022 - Issue 3-4
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Short Report

A case of juvenile-onset amyotrophic lateral sclerosis with a de novo frameshift FUS gene mutation presenting with bilateral abducens palsy

Ying WuDepartment of Neurology, Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatric, West China Hospital, Sichuan University, Chengdu, ChinaView further author information
,
Chunyu LiDepartment of Neurology, Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatric, West China Hospital, Sichuan University, Chengdu, ChinaView further author information
,
Tianmi YangDepartment of Neurology, Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatric, West China Hospital, Sichuan University, Chengdu, ChinaView further author information
,
Junyu LinDepartment of Neurology, Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatric, West China Hospital, Sichuan University, Chengdu, ChinaView further author information
&
Huifang ShangDepartment of Neurology, Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatric, West China Hospital, Sichuan University, Chengdu, ChinaCorrespondence[email protected]
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Pages 313-314 | Received 24 Feb 2021, Accepted 02 May 2021, Published online: 02 Jun 2021

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Read on this site (1)

Ting Lu, Jie Yang, Lijun Luo & Dongsheng Wei. (2022) FUS mutations in Asian amyotrophic lateral sclerosis patients: a case report and literature review of genotype-phenotype correlations. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 23:7-8, pages 580-584.
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Articles from other publishers (1)

Peishan WangQiao WeiHongfu LiZhi-Ying Wu. (2023) Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations. Chinese Medical Journal 136:2, pages 176-183.
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