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GSTM1 copy number variation in the context of single nucleotide polymorphisms in the human GSTM cluster
BACKGROUND: GSTM1 gene deletion is one of the most known copy number polymorphisms in human genome. It is most likely caused by homologous recombination between the repeats flanking the gene. However, taking into account that the deletion has no crucial effects on human well-being, and the ability o...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837583/ https://www.ncbi.nlm.nih.gov/pubmed/27099630 http://dx.doi.org/10.1186/s13039-016-0241-0 |