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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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| Foilsithe in: | Eur J Hum Genet |
|---|---|
| Main Authors: | , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Springer International Publishing
2018
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| Ábhair: | |
| Rochtain Ar Líne: | 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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