A comprehensive analysis of copy number variation in a Turkish dementia cohort

A comprehensive analysis of copy number variation in a Turkish dementia cohort

Abstract Background Copy number variants (CNVs) include deletions or multiplications spanning genomic regions. These regions vary in size and may span genes known to play a role in human diseases. As examples, duplications and triplications of SNCA have been shown to cause forms of Parkinson’s disea...

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Bibliographic Details
Main Authors: Nadia Dehghani, Gamze Guven, Celia Kun-Rodrigues, Catarina Gouveia, Kalina Foster, Hasmet Hanagasi, Ebba Lohmann, Bedia Samanci, Hakan Gurvit, Basar Bilgic, Jose Bras, Rita Guerreiro
Format: Article
Language:English
Published: BMC 2021-07-01
Series:Human Genomics
Subjects:
Copy number variants
Dementia
Genotyping
Online Access:https://doi.org/10.1186/s40246-021-00346-z

Internet

https://doi.org/10.1186/s40246-021-00346-z

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