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Functional Characterization of SCN10A Variants in Several Cases of Sudden Unexplained Death
BACKGROUND: Multiple genome-wide association studies (GWAS) and targeted gene sequencing have identified common variants in SCN10A in cases of PR and QRS duration abnormalities, atrial fibrillation and Brugada syndrome. The New York City Office of Chief Medical Examiner has now also identified five...
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| Publicado en: | Forensic Sci Int |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6625669/ https://ncbi.nlm.nih.gov/pubmed/31195250 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.forsciint.2019.05.042 |
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