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Haplotype Analysis of the First A4V-SOD1 Spanish Family: Two Separate Founders or a Single Common Founder?
Despite the genetic heterogeneity reported in familial amyotrophic lateral sclerosis (ALS) (fALS), Cu/Zn superoxide-dismutase (SOD1) gene mutations are the second most common cause of the disease, accounting for around 20% of all families (ALS1) and isolated sporadic cases (sALS). At least 186 diffe...
Autores principales: | Garcia, Cecilia, Vidal-Taboada, Jose Manuel, Syriani, Enrique, Salvado, Maria, Morales, Miguel, Gamez, Josep |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857184/ https://www.ncbi.nlm.nih.gov/pubmed/31781168 http://dx.doi.org/10.3389/fgene.2019.01109 |
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