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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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| 主要な著者: | , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2011
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| 主題: | |
| オンライン･アクセス: | 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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