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The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most
We illustrate the work necessary to reverse course after identification of a KCNQ1 variant interpreted erroneously as causing long QT syndrome (LQTS) and to identify the true cause of a case of sudden death in the young. Surrogate genetic testing of a decedent’s living brother identified a rare KCNQ...
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| Foilsithe in: | Mayo Clin Proc |
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| Main Authors: | , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2016
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6365209/ https://ncbi.nlm.nih.gov/pubmed/27810088 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mayocp.2016.08.008 |
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