Screening of novel restless legs syndrome–associated genes in French-Canadian families

OBJECTIVE: To examine whether any rare, protein-altering variants could be identified across 13 recently identified restless legs syndrome (RLS) loci in familial French-Canadian cases. METHODS: Whole-exome sequences from 7 large French-Canadian families (4–8 affected per family for a total of 38 cas...

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Detalles Bibliográficos
Autores principales: Akçimen, Fulya, Spiegelman, Dan, Dionne-Laporte, Alexandre, Gan-Or, Ziv, Dion, Patrick A., Rouleau, Guy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305992/
https://www.ncbi.nlm.nih.gov/pubmed/30637332
http://dx.doi.org/10.1212/NXG.0000000000000296

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305992/
https://www.ncbi.nlm.nih.gov/pubmed/30637332
http://dx.doi.org/10.1212/NXG.0000000000000296

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