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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...
Gardado en:
| Publicado en: | J Clin Med |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
MDPI
2019
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| Assuntos: | |
| Acceso en liña: | 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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