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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Detalles Bibliográficos
Autores principales: Stephanou, Coralea, Tamana, Stella, Minaidou, Anna, Papasavva, Panayiota, Kleanthous, Marina, Kountouris, Petros
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912721/
https://www.ncbi.nlm.nih.gov/pubmed/31717530
http://dx.doi.org/10.3390/jcm8111927

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912721/
https://www.ncbi.nlm.nih.gov/pubmed/31717530
http://dx.doi.org/10.3390/jcm8111927

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