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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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| Pubblicato in: | Stroke |
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| Autori principali: | , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2020
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| Soggetti: | |
| Accesso online: | 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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