Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation
Author:
Affiliation:
1. Department of Medical, Surgical and Neurological Sciences, University of Siena, Siena, Italy and
2. Pneumology Unit, Università Cattolica del Sacro Cuore, Rome, Italy
Funder
University of Siena
Publisher
Informa UK Limited
Subject
Clinical Neurology,Neurology
Link
https://www.tandfonline.com/doi/pdf/10.1080/21678421.2019.1621345
Reference13 articles.
1. ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics
2. Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene
3. D90A-SOD1 mediated amyotrophic lateral sclerosis: A single founder for all cases with evidence for aCis-acting disease modifier in the recessive haplotype
4. Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients
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3. A Systematic Review of Genotype–Phenotype Correlation across Cohorts Having Causal Mutations of Different Genes in ALS;Journal of Personalized Medicine;2020-06-29
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