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Article

A Novel Genetic Marker for the C9orf72 Repeat Expansion in the Finnish Population.

Journal of Alzheimer's disease : JAD - 1 Jan 2021

Rostalski Hannah, Korhonen Ville, Kuulasmaa Teemu, Solje Eino, Krüger Johanna, Gen Finn, Kaivola Karri, Eide Per Kristian, Lambert Jean-Charles, Julkunen Valtteri, Tienari Pentti J, Remes Anne M, Leinonen Ville, Hiltunen Mikko, Haapasalo Annakaisa

Abstract excerpt

BACKGROUND: C9orf72 repeat expansion (C9exp) is the most common genetic cause underlying frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS). However, detection of the C9exp requires elaborative methods. OBJECTIVE: Identification of C9exp carriers from genotyped cohorts could be facilitated by using single nucleotide polymorphisms (SNPs) as markers for the C9exp. METHODS: We...

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Identifiers

PMID: 34397416
DOI: 10.3233/JAD-210599

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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