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

Abstract 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 d...

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Номзүйн дэлгэрэнгүй

Үндсэн зохиолчид:	Zied Landoulsi, Sawssan Benromdhan, Mouna Ben Djebara, Mariem Damak, Hamza Dallali, Rym Kefi, Sonia Abdelhak, Amina Gargouri-Berrechid, Chokri Mhiri, Riadh Gouider
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	BMC 2017-07-01
Цуврал:	BMC Medical Genetics
Нөхцлүүд:	Parkinson’s disease LRRK2 gene G2019S KASP genetic testing
Онлайн хандалт:	http://link.springer.com/article/10.1186/s12881-017-0432-5
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!