In silico analysis of single nucleotide polymorphism (SNPs) in human β-globin gene.
Single amino acid substitutions in the globin chain are the most common forms of genetic variations that produce hemoglobinopathies--the most widespread inherited disorders worldwide. Several hemoglobinopathies result from homozygosity or compound heterozygosity to beta-globin (HBB) gene mutations,...
Guardado en:
Autores principales: | Mohammed Alanazi, Zainularifeen Abduljaleel, Wajahatullah Khan, Arjumand S Warsy, Mohamed Elrobh, Zahid Khan, Abdullah Al Amri, Mohammad D Bazzi |
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Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2011
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Materias: | |
Acceso en línea: | https://doaj.org/article/c5a78ccafb8746ad93873c1589c2eb90 |
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