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...

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Detalles Bibliográficos
Autores principales: Gentile, Giulia, Perrone, Benedetta, Morello, Giovanna, Simone, Isabella Laura, Andò, Sebastiano, Cavallaro, Sebastiano, Conforti, Francesca Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701978/
https://www.ncbi.nlm.nih.gov/pubmed/34946792
http://dx.doi.org/10.3390/genes12121843

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