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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Dettagli Bibliografici
Pubblicato in:PLoS One
Autori principali: Odgerel, Zagaa, Sonti, Shilpa, Hernandez, Nora, Park, Jemin, Ottman, Ruth, Louis, Elan D., Clark, Lorraine N.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2019
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6690583/
https://ncbi.nlm.nih.gov/pubmed/31404076
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0220512
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