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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Detalles Bibliográficos
Autores principales: Landoulsi, Zied, Benromdhan, Sawssan, Ben Djebara, Mouna, Damak, Mariem, Dallali, Hamza, Kefi, Rym, Abdelhak, Sonia, Gargouri-Berrechid, Amina, Mhiri, Chokri, Gouider, Riadh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501550/
https://www.ncbi.nlm.nih.gov/pubmed/28683740
http://dx.doi.org/10.1186/s12881-017-0432-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501550/
https://www.ncbi.nlm.nih.gov/pubmed/28683740
http://dx.doi.org/10.1186/s12881-017-0432-5

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