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A Genotype-First Approach to Defining the Subtypes of a Complex Disease
Medical genetics typically entails the detailed characterization of a patient’s phenotypes followed by genotyping to discover the responsible gene or mutation. Here, we propose that the systematic discovery of genetic variants associated with complex diseases such as autism are progressing to a poin...
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| Glavni autori: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2014
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4076166/ https://ncbi.nlm.nih.gov/pubmed/24581488 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2014.02.002 |
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