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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Detalhes bibliográficos
Publicado no:Mol Cytogenet
Main Authors: Khrunin, Andrey V., Filippova, Irina N., Aliev, Aydar M., Tupitsina, Tat’yana V., Slominsky, Petr A., Limborska, Svetlana A.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Research
Acesso em linha: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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