A Genome-Wide Association Study Identifies UTRN Gene Polymorphism for Restless Legs Syndrome in a Korean Population

OBJECTIVE: Restless legs syndrome (RLS) is a highly heritable and common neurological sensorimotor disease disturbing sleep. The objective of study was to investigate significant gene for RLS by performing GWA and replication study in a Korean population. METHODS: We performed a GWA study for RLS sy...

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Detalles Bibliográficos
Autores principales: Cho, Chul-Hyun, Choi, Ji-Hye, Kang, Seung-Gul, Yoon, Ho-Kyoung, Park, Young-Min, Moon, Joung-Ho, Jung, Ki-Young, Han, Jin-Kyu, Shin, Hong-Bum, Noh, Hyun Ji, Koo, Yong Seo, Kim, Leen, Woo, Hyun Goo, Lee, Heon-Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neuropsychiatric Association 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714726/
https://www.ncbi.nlm.nih.gov/pubmed/29209388
http://dx.doi.org/10.4306/pi.2017.14.6.830

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714726/
https://www.ncbi.nlm.nih.gov/pubmed/29209388
http://dx.doi.org/10.4306/pi.2017.14.6.830

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