Evaluation of High Resolution Melting analysis as an alternate tool to screen for risk alleles associated with small kidneys in Indian newborns

BACKGROUND: Single nucleotide polymorphisms (SNPs) are the most common forms of sequence variations in the human genome. They contribute to the human phenotypic spectrum and are associated with variations in response to pathogens, drugs and vaccines. Recently, SNPs in three human genes involved in k...

Descripción completa

Detalles Bibliográficos
Autores principales: Raghavendra, Ashwini, Siji, Annes, Sridhar, TS, Phadke, Kishore, Vasudevan, Anil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219565/
https://www.ncbi.nlm.nih.gov/pubmed/22035350
http://dx.doi.org/10.1186/1471-2369-12-60

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219565/
https://www.ncbi.nlm.nih.gov/pubmed/22035350
http://dx.doi.org/10.1186/1471-2369-12-60

Ejemplares similares