A novel tetra-primer ARMS-PCR for genotyping of the OPRM1 gene rs1799971 variant associated with opioid use disorders

OBJECTIVES: A SNV is a single nucleotide change that can occur at any point in the genome. SNVs are the most common genetic variants that occur in the human genome, and a number of SNVs have been found to be associated with human traits and disease. Researchers genotype SNVs using TaqMan technology,...

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Detalles Bibliográficos
Autores principales: Wijekumar, P. J., Ranadeva, N. D.K., Jayamaha, A. R., Herath, H. M.N.D.M., Noorden, N., Fernando, S. S.N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10648702/
https://www.ncbi.nlm.nih.gov/pubmed/37964305
http://dx.doi.org/10.1186/s13104-023-06578-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10648702/
https://www.ncbi.nlm.nih.gov/pubmed/37964305
http://dx.doi.org/10.1186/s13104-023-06578-7

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