Whole genome sequencing and rare variant analysis in essential tremor families

Essential tremor (ET) is one of the most common movement disorders. The etiology of ET remains largely unexplained. Whole genome sequencing (WGS) is likely to be of value in understanding a large proportion of ET with Mendelian and complex disease inheritance patterns. In ET families with Mendelian...

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Detalles Bibliográficos
Autores principales: Odgerel, Zagaa, Sonti, Shilpa, Hernandez, Nora, Park, Jemin, Ottman, Ruth, Louis, Elan D., Clark, Lorraine N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690583/
https://www.ncbi.nlm.nih.gov/pubmed/31404076
http://dx.doi.org/10.1371/journal.pone.0220512

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690583/
https://www.ncbi.nlm.nih.gov/pubmed/31404076
http://dx.doi.org/10.1371/journal.pone.0220512

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