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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Main Authors: Alanazi, Mohammed, Abduljaleel, Zainularifeen, Khan, Wajahatullah, Warsy, Arjumand S., Elrobh, Mohamed, Khan, Zahid, Amri, Abdullah Al, Bazzi, Mohammad D.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2011
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3197589/
https://ncbi.nlm.nih.gov/pubmed/22028795
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0025876
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