Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort

BACKGROUND: In North African populations, G2019S mutation in LRRK2 gene, encoding for the leucine-rich repeat kinase 2, is the most prevalent mutation linked to familial and sporadic Parkinson’s disease (PD). Early detection of G2019S by fast genetic testing is very important to guide PD’s diagnosis...

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Udgivet i:BMC Med Genet
Main Authors: Landoulsi, Zied, Benromdhan, Sawssan, Ben Djebara, Mouna, Damak, Mariem, Dallali, Hamza, Kefi, Rym, Abdelhak, Sonia, Gargouri-Berrechid, Amina, Mhiri, Chokri, Gouider, Riadh
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2017
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5501550/
https://ncbi.nlm.nih.gov/pubmed/28683740
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-017-0432-5
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