Cargando...
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...
Guardado en:
| Publicado en: | Mol Cytogenet |
|---|---|
| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2016
|
| Materias: | |
| Acceso en línea: | 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 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|