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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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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Odgerel, Zagaa, Sonti, Shilpa, Hernandez, Nora, Park, Jemin, Ottman, Ruth, Louis, Elan D., Clark, Lorraine N.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2019
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Acesso em linha: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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