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A stroke gene panel for whole-exome sequencing

Extensive analyses of known monogenic causes of stroke by whole-exome/genome sequencing are technically possible today. We here aimed to compile a comprehensive panel of genes associated with monogenic causes of stroke for use in clinical and research situations. We systematically searched the publi...

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Detalhes bibliográficos
Publicado no:Eur J Hum Genet
Main Authors: Ilinca, Andreea, Samuelsson, Sofie, Piccinelli, Paul, Soller, Maria, Kristoffersson, Ulf, Lindgren, Arne G.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer International Publishing 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6336868/
https://ncbi.nlm.nih.gov/pubmed/30356112
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-018-0274-4
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