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Novel genetic therapeutic approaches for modulating the severity of β-thalassemia (Review)

Thalassemia is a genetic haematological disorder that arises due to defects in the α and β-globin genes. Worldwide, 0.3-0.4 million children are born with haemoglobinopathies per year. Thalassemic patients, as well as their families, face various serious clinical, socio-economic, and psychosocial ch...

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Detalles Bibliográficos
Autores principales:	Amjad, Fareeha, Fatima, Tamseel, Fayyaz, Tuba, Khan, Muhammad Aslam, Qadeer, Muhammad Imran
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2020
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484974/ https://www.ncbi.nlm.nih.gov/pubmed/32953110 http://dx.doi.org/10.3892/br.2020.1355

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