Abstract
Two alleles of the calcitonin receptor gene exist: a base mutation T->C in the third intracellular C-terminal domain changes a proline (CCG) to a leucine (CTG). The Codon 447 polymorphism of CTR gene was studied in 9 normal unrelated individuals from South India. The genomic DNA was isolated, CTR gene was amplified and the PCR products were subjected to restriction digestion. We have found that the C/T alleles show a 33.33% indicating that the individuals are protected against calcium related disorders.
| Original language | English |
|---|---|
| Pages (from-to) | 273-276 |
| Number of pages | 4 |
| Journal | International Journal of Human Genetics |
| Volume | 8 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Sep 2008 |
| Externally published | Yes |
Keywords
- Calcitonin receptor gene
- Polymorphisms
- SNP