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...

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Vydáno v:Mol Cytogenet
Hlavní autoři: Khrunin, Andrey V., Filippova, Irina N., Aliev, Aydar M., Tupitsina, Tat’yana V., Slominsky, Petr A., Limborska, Svetlana A.
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2016
Témata:
Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4837583/
https://ncbi.nlm.nih.gov/pubmed/27099630
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-016-0241-0
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