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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Detalles Bibliográficos
Autores principales: Khrunin, Andrey V., Filippova, Irina N., Aliev, Aydar M., Tupitsina, Tat’yana V., Slominsky, Petr A., Limborska, Svetlana A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
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

Internet

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

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