Significance of genetic modifiers of hemoglobinopathies leading towards precision medicine

Hemoglobinopathies though a monogenic disorder, show phenotypic variability. Hence, understanding the genetics underlying the heritable sub-phenotypes of hemoglobinopathies, specific to each population, would be prognostically useful and could inform personalized therapeutics. This study aimed to ev...

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Detalles Bibliográficos
Autores principales: Hariharan, Priya, Gorivale, Manju, Sawant, Pratibha, Mehta, Pallavi, Nadkarni, Anita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536722/
https://www.ncbi.nlm.nih.gov/pubmed/34686692
http://dx.doi.org/10.1038/s41598-021-00169-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536722/
https://www.ncbi.nlm.nih.gov/pubmed/34686692
http://dx.doi.org/10.1038/s41598-021-00169-x

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