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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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Detalles Bibliográficos
Publicado en:J Clin Med
Main Authors: Stephanou, Coralea, Tamana, Stella, Minaidou, Anna, Papasavva, Panayiota, Kleanthous, Marina, Kountouris, Petros
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2019
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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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