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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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Bibliografiske detaljer
Udgivet i:PLoS One
Main Authors: Odgerel, Zagaa, Sonti, Shilpa, Hernandez, Nora, Park, Jemin, Ottman, Ruth, Louis, Elan D., Clark, Lorraine N.
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2019
Fag:
Online adgang: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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