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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Bibliographic Details
Main Authors: Ylenia Barbanera, Francesco Arcioni, Hovirag Lancioni, Roberta La Starza, Irene Cardinali, Caterina Matteucci, Valeria Nofrini, Antonella Roetto, Antonio Piga, Paola Grammatico, Maurizio Caniglia, Cristina Mecucci, Paolo Gorello
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0240632