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Beta Thalassemia and Klinefelter syndrome: a rare occurrence
Abstract Background β-Thalassemia is an inherited haematological blood disorder in the HBB gene, and variations in this HBB gene lead to the absence/deficiency of the Beta chain synthesis of haemoglobin leading to severe anaemia. Klinefelter syndrome is a chromosomal abnormality that affects physica...
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Main Authors: | , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
SpringerOpen
2022-05-01
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Colecção: | Egyptian Journal of Medical Human Genetics |
Assuntos: | |
Acesso em linha: | https://doi.org/10.1186/s43042-022-00300-1 |
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