Genetics landscape of nonsyndromic hearing loss in Indian populations

M Ray, S Sarkar, MN Sable - Journal of Pediatric Genetics, 2022 - thieme-connect.com
Congenital nonsyndromic hearing loss (NSHL) has been considered as one of the most
prevalent chronic disorder in children. It affects the physical and mental conditions of a large …

Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India

PK Singh, M Ghosh, S Sharma, S Shastri… - Indian Journal of …, 2017 - journals.lww.com
Methods: Forty seven families including 26 consanguineous families with at least two
hearing impaired children and one normal hearing child and 21 non-consanguineous …

KARYOTYPE STUDY IN PATIENTS WITH HEARING DISABILITY

HB Rajput, SM Ruparel, HR Jadav, CA Pensi - National Journal of Medical …, 2012 - njmr.in
Background: Hearing disability is the most common sensory disorder in humans. About 50%
cases of congenital hearing loss are due to genetic causes. About 70% of genetic hearing …