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ALS in Finland: Major Genetic Variants and Clinical Characteristics of Patients With and Without the C9orf72 Hexanucleotide Repeat Expansion.

Hannu LaaksovirtaJyrki LaunesLilja JanssonBryan J TraynorKarri KaivolaPentti J Tienari
Published in: Neurology. Genetics (2022)
was also found among patients with sporadic ALS. The enrichment of these 2 variants likely contributes to the high incidence of ALS in Finland.
Keyphrases
  • amyotrophic lateral sclerosis
  • risk factors
  • copy number