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...

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Detalles Bibliográficos
Autores principales: Zhao, Yongzhong, Marotta, Michael, Eichler, Evan E., Eng, Charis, Tanaka, Hisashi
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Research Article
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

Internet

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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