Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study

The hemoglobin disorders are the most common single gene disorders in the world. Previous studies have suggested that they are deeply geographically structured and a variety of genetic determinants influences different clinical phenotypes between patients inheriting identical β-globin gene mutations...

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Detalles Bibliográficos
Autores principales: Barbanera, Ylenia, Arcioni, Francesco, Lancioni, Hovirag, La Starza, Roberta, Cardinali, Irene, Matteucci, Caterina, Nofrini, Valeria, Roetto, Antonella, Piga, Antonio, Grammatico, Paola, Caniglia, Maurizio, Mecucci, Cristina, Gorello, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581000/
https://www.ncbi.nlm.nih.gov/pubmed/33091040
http://dx.doi.org/10.1371/journal.pone.0240632

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