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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 21, 2020 - Issue 5-6
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Letter

An exon 5 mutation (c.425G>C, p.Gly141Ala) in the SOD1 gene in a Chinese family associated with incomplete penetrance

Si-Qi DongDepartment of Neurology, Huashan Hospital, Fudan University, Shanghai, China, View further author information
,
Xiao-Ni LiuDepartment of Neurology, Huashan Hospital, Fudan University, Shanghai, China, ;Institute of Neurology, Fudan University, Shanghai, China, View further author information
,
Wen-Bo YangDepartment of Neurology, Huashan Hospital, Fudan University, Shanghai, China, View further author information
,
Yan-Ni ZhouDepartment of Neurology, Huashan Hospital, Fudan University, Shanghai, China, ;Department of Anthropology and Human Genetics, School of Life Sciences, Fudan University, Shanghai, China, ;Human Phenome Institute, Fudan University, Shanghai, ChinaView further author information
,
Jiu-Cun WangDepartment of Anthropology and Human Genetics, School of Life Sciences, Fudan University, Shanghai, China, ;Human Phenome Institute, Fudan University, Shanghai, ChinaView further author information
&
Xiang-Jun ChenDepartment of Neurology, Huashan Hospital, Fudan University, Shanghai, China, ;Institute of Neurology, Fudan University, Shanghai, China, ;Human Phenome Institute, Fudan University, Shanghai, ChinaCorrespondence[email protected]
View further author information
Pages 473-476 | Received 29 Dec 2019, Accepted 23 Feb 2020, Published online: 15 Mar 2020

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