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Genetic Modifiers at the Crossroads of Personalised Medicine for Haemoglobinopathies
Haemoglobinopathies are common monogenic disorders with diverse clinical manifestations, partly attributed to the influence of modifier genes. Recent years have seen enormous growth in the amount of genetic data, instigating the need for ranking methods to identify candidate genes with strong modify...
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| Publicado no: | J Clin Med |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6912721/ https://ncbi.nlm.nih.gov/pubmed/31717530 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm8111927 |
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