The risks of RELN polymorphisms and its expression in the development of otosclerosis

The risks of RELN polymorphisms and its expression in the development of otosclerosis

Show other versions (1)

Otosclerosis (OTSC) is the primary form of conductive hearing loss characterized by abnormal bone remodelling within the otic capsule of the human middle ear. A genetic association of the RELN SNP rs3914132 with OTSC has been identified in European population. Previously, we showed a trend towards a...

Full description

Bibliographic Details
Main Authors: Saurabh Priyadarshi, Kirtal Hansdah, Neha Singh, Amal Bouzid, Chinmay Sundar Ray, Khirod Chandra Panda, Narayan Chandra Biswal, Ashim Desai, Jyotish Chandra Choudhury, Adel Tekari, Saber Masmoudi, Puppala Venkat Ramchander
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2022-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165908/?tool=EBI

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165908/?tool=EBI

Similar Items