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Artigo Acesso aberto Revisado por pares

Cathrine Goberg Olsen, Øyvind L. Busk, Tori Navestad Aanjesen, Karl Bjørnar Alstadhaug, Ingrid Kristine Bjørnå, Geir J. Braathen, Kristin Lif Breivik, Natasha Demic, Heidi Øyen Flemmen, Erika Hallerstig, Ineke Hogenesch, Øystein L. Holla, Anne Berit Jøntvedt, Margitta T. Kampman, Grethe Kleveland, Helene Ballo Kvernmo, Unn Ljøstad, Angelina Maniaol, Åse Hagen Morsund, Ola Nakken, Camilla Novy, Tiina Rekand, Katrin Schlüter, Stephan Schüler, Kristian Tveten, Ole‐Bjørn Tysnes, Trygve Holmøy, Helle Høyer,

<b><i>Background:</i></b> Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that affects motor neurons. In Europe, disease-causing genetic variants have been identified in 40–70% of familial ALS patients and approximately 5% of sporadic ALS patients. In Norway, the contribution of genetic variants to ALS has not yet been studied. In light of the potential development of personalized medicine, knowledge of the genetic causes of ALS in a population is becoming ...

Tópico(s): Neurological diseases and metabolism

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