Recent Studies on Genetic Mutations

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Exploring the Neurobiological Mechanisms of Fragile X Syndrome

Introduction FXS is the only known cause of intellectual disability, being primarily inherited as well as being one of the major genetic autism spectrum disorders. This results from a mutation...

Advancements in Iron Chelation Therapy for Thalassemia Patients

Introduction Thalassemia is one of the blood disorders passed on to the offspring in which the human body fails to make enough hemoglobin for proper oxygen uptake. The treatment mostly...

Innovations in DNA Cloning and Sequencing

Introduction DNA cloning and sequencing have been an overwhelming game-changing field in the past 50 years, establishing our knowledge of genetics as well as enabling even more scientific discoveries. Together,...

Genetic and Molecular Insights into Sickle Cell Disease

Sickle cell disease is a congenital disease of the blood that has presented a lot of complications to researchers due to its peculiarity, particularly among the Black African fraternity. What...

Advancements in CFTR Modulators for Cystic Fibrosis Treatment

Cystic fibrosis is one of the hereditary diseases that run through genetics and, until now, was one of the biggest challenges to patients and doctors. This germinal multicystic illness with...

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