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

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An exon 5 mutation (c.425G>C, p.Gly141Ala) in the SOD1 gene in a Chinese family associated with incomplete penetrance.
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ( IF 2.8 ) Pub Date : 2020-03-15 , DOI: 10.1080/21678421.2020.1738496
Si-Qi Dong ₁ , Xiao-Ni Liu _{1,

2} , Wen-Bo Yang ₁ , Yan-Ni Zhou _{1,

3,

4} , Jiu-Cun Wang _{3,

4} , Xiang-Jun Chen _{1,

2,

4}

Affiliation

(2020). An exon 5 mutation (c.425G>C, p.Gly141Ala) in the SOD1 gene in a Chinese family associated with incomplete penetrance. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration: Vol. 21, No. 5-6, pp. 473-476.

更新日期：2020-03-15

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