Addressing the routine failure to clinically identify monogenic cases of common disease
Abstract Changes in medical practice are needed to improve the diagnosis of monogenic forms of selected common diseases. This article seeks to focus attention on the need for universal genetic testing in common diseases for which the recommended clinical management of patients with specific monogeni...
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| Hauptverfasser: | , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMC
2022-06-01
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| Schriftenreihe: | Genome Medicine |
| Online-Zugang: | https://doi.org/10.1186/s13073-022-01062-6 |
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