Individual Oligogenic Background in p.D91A-<i>SOD1</i> Amyotrophic Lateral Sclerosis Patients
The p.D91A is one of the most common ALS-causing <i>SOD1</i> mutations and is known to be either recessive or dominant. The homozygous phenotype is characterized by prolonged survival and slow progression of disease, whereas the affected heterozygous phenotypes can vary. To date, no gene...
Main Authors: | Giulia Gentile, Benedetta Perrone, Giovanna Morello, Isabella Laura Simone, Sebastiano Andò, Sebastiano Cavallaro, Francesca Luisa Conforti |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-11-01
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Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/12/12/1843 |
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