Loss of RTN4RL2 disrupts synapse formation and function between inner hair cells and spiral ganglion neurons, leading to elevated auditory thresholds and highlighting its critical role in hearing.
The Brighterside of News on MSN
Researchers discover genetic cause of hearing loss and identify possible treatments
Researchers have understood for decades that some forms of deafness are inherited, yet until now, few of those genetic clues ...
University of Oklahoma Researcher Investigates Speech Acquisition in Children with Cochlear Implants
Matthew Masapollo studies how children with hearing impairments learn speech, highlighting the role of tactile feedback.
Sungkyunkwan University Samsung Changwon Hospital has successfully performed a cochlear implant surgery for a Nepalese child ...
MedPage Today on MSN
Gene Therapy Restores Hearing for Rare Cause of Congenital Deafness
In a small pivotal trial of an investigational gene therapy, most cases of congenital profound deafness from genetic variants ...
In theory I should love Parliament House in Canberra, because I am a boorishly boring political nerd, a debating devotee and ...
Nearly all participants (11 of 12) experienced clinically meaningful hearing improvements, including three who achieved normal hearing; eight ...
Detailed price information for Envoy Medical Inc (COCH-Q) from The Globe and Mail including charting and trades.
Newspoint on MSN
Doctors Perform Rare Laryngeal Reinnervation Surgery to Restore Voice Lost for Six Months
A team of doctors at Sarvodaya Hospital, Sector 8, Faridabad, successfully performed a rare and complex laryngeal ...
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