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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,...

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Detalles Bibliográficos
Autores principales:	Alanazi, Mohammed, Abduljaleel, Zainularifeen, Khan, Wajahatullah, Warsy, Arjumand S., Elrobh, Mohamed, Khan, Zahid, Amri, Abdullah Al, Bazzi, Mohammad D.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2011
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3197589/ https://www.ncbi.nlm.nih.gov/pubmed/22028795 http://dx.doi.org/10.1371/journal.pone.0025876

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