Genotype-phenotype correlation of HbH disease in northern Iraq
Abstract Background HbH disease results from dysfunction of three, less commonly two, α-globin genes through various combinations of deletion and non-deletion mutations. Characterization of the mutations and the underlying genotypes is fundamental for proper screening and prevention of thalassaemia...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2020-10-01
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| coleção: | BMC Medical Genetics |
| Assuntos: | |
| Acesso em linha: | http://link.springer.com/article/10.1186/s12881-020-01141-8 |
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