Whole exome sequencing in 22 young ischemic stroke patients with familial clustering of stroke

BACKGROUNDS AND PURPOSE: Although new methods for genetic analyses are rapidly evolving, there are currently knowledge gaps in how to detect Mendelian forms of stroke. METHODS: We performed whole exome sequencing (WES) in 22 probands, under 56 years at their first ischemic stroke episode, from multi...

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Detalhes bibliográficos
Publicado no:Stroke
Main Authors: Ilinca, Andreea, Martinez-Majander, Nicolas, Samuelsson, Sofie, Piccinelli, Paul, Truvé, Katarina, Cole, John, Kittner, Steven, Soller, Maria, Kristoffersson, Ulf, Tatlisumak, Turgut, Puschmann, Andreas, Putaala, Jukka, Lindgren, Arne
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7584402/
https://ncbi.nlm.nih.gov/pubmed/32172663
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/STROKEAHA.119.027474
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