Lack of association between SNP rs3914132 of the RELN gene and otosclerosis in India.

@article{Priyadarshi2010LackOA,
  title={Lack of association between SNP rs3914132 of the RELN gene and otosclerosis in India.},
  author={Saurabh Priyadarshi and Khirod Chandra Panda and Ashok Kumar Panda and Puppala Venkat Ramchander},
  journal={Genetics and molecular research : GMR},
  year={2010},
  volume={9 3},
  pages={1914-20}
}
Otosclerosis (MIM 166800) is primarily a metabolic bone disorder of the otic capsule, which leads to bony fixation of the stapedial footplate in the oval window; it is among the most common causes of acquired hearing loss. The etiology of this disease is largely unknown, although epidemiological studies suggest the involvement of both genetic and… CONTINUE READING