Beyond C9orf72: repeat expansions and copy number variations as risk factors of amyotrophic lateral sclerosis across various populations

Beyond C9orf72: repeat expansions and copy number variations as risk factors of amyotrophic lateral sclerosis across various populations

Abstract Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder which is characterized by the loss of both upper and lower motor neurons in the central nervous system. In a significant fraction of ALS cases - irrespective of family history- a genetic background may be identified. The ge...

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Bibliographic Details
Main Authors: Zsófia Flóra Nagy, Margit Pál, József I. Engelhardt, Mária Judit Molnár, Péter Klivényi, Márta Széll
Format: Article
Language:English
Published: BMC 2024-01-01
Series:BMC Medical Genomics
Subjects:
Amyotrophic lateral sclerosis
ALS
ALS genetics
Intermediate length repeat expansion
Copy number variation
ATXN1
Online Access:https://doi.org/10.1186/s12920-024-01807-9

Internet

https://doi.org/10.1186/s12920-024-01807-9

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