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Individual Oligogenic Background in p.D91A-SOD1 Amyotrophic Lateral Sclerosis Patients
The p.D91A is one of the most common ALS-causing SOD1 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 genetic protective fact...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701978/ https://www.ncbi.nlm.nih.gov/pubmed/34946792 http://dx.doi.org/10.3390/genes12121843 |