0000000001262399

AUTHOR

Renato Messina

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A Particular Focus on the Prevalence of α- and β-Thalassemia in Western Sicilian Population from Trapani Province in the COVID-19 Era

2023

Thalassemia is a Mendelian inherited blood disease caused by α- and β-globin gene mutations, known as one of the major health problems of Mediterranean populations. Here, we examined the distribution of α- and β-globin gene defects in the Trapani province population. A total of 2,401 individuals from Trapani province were enrolled from January 2007 to December 2021, and routine methodologies were used for detecting the α- and β-globin genic variants. Appropriate analysis was also performed. Eight mutations in the α globin gene showed the highest frequency in the sample studied; three of these genetic variants represented the 94% of the total α-th…

thalassemiagenotypeOrganic Chemistryphenotype in the diagnosisGeneral MedicineTrapani population<i>α-</i> and <i>β-globin</i> genes defectsCatalysisComputer Science ApplicationsInorganic ChemistryPhysical and Theoretical ChemistryMolecular Biologyα- and β-globin genes defectSpectroscopyphenotype in the diagnosi
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