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

Subjects

Subjects :

GENE families
MOTOR unit
GENETIC mutation
AMYOTROPHIC lateral sclerosis
MEDICAL genetics

Details

Language :

English

ISSN :

21678421

Volume :

21

Issue :

5/6

Database :

Complementary Index

Journal :

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration

Publication Type :

Academic Journal

Accession number :

145431727

Full Text :

https://doi.org/10.1080/21678421.2020.1738496