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Digenic inheritance in medical genetics
Digenic inheritance (DI) is the simplest form of inheritance for genetically complex diseases. By contrast with the thousands of reports that mutations in single genes cause human diseases, there are only dozens of human disease phenotypes with evidence for DI in some pedigrees. The advent of high-t...
Tallennettuna:
| Päätekijä: | |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Publishing Group
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3778050/ https://ncbi.nlm.nih.gov/pubmed/23785127 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2013-101713 |
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