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Linkage Disequilibrium between Two High-Frequency Deletion Polymorphisms: Implications for Association Studies Involving the glutathione-S transferase (GST) Genes
Copy number variations (CNVs) represent a large source of genetic variation in humans and have been increasingly studied for disease association. A deletion polymorphism of the gene encoding the cytosolic detoxification enzyme glutathione S-transferase theta 1 (GSTT1) has been extensively studied fo...
Autores principales: | Zhao, Yongzhong, Marotta, Michael, Eichler, Evan E., Eng, Charis, Tanaka, Hisashi |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2672168/ https://www.ncbi.nlm.nih.gov/pubmed/19424424 http://dx.doi.org/10.1371/journal.pgen.1000472 |
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