The most common form of hereditary deafness in humans is caused by mutations in the GJB2 gene, which encodes the gap junction protein connexin 26. That regulates the transport of potassium and ...
Sensorion receives DMC recommendation to continue the Audiogene phase 1/2 trial of SENS-501: Montpellier, France Monday, February 24, 2025, 18:00 Hrs [IST] Sensorion, a pioneering ...
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GlobalData on MSNSensorion’s Phase I/II gene therapy trial to continue with DMC recommendationSensorion's Audiogene Phase I/II trial of the SENS-501 gene therapy programme has received a favourable recommendation from ...
Regulatory News: Sensorion (FR0012596468 ? ALSEN) a pioneering clinical-stage biotechnology company specializing in the development of novel therapies to restore, treat and prevent hearing loss ...
WHO has published a new technical brief on encephalitis , a serious, life-threatening neurological condition characterized by ...
Breaking this down by channel, U.S. retail net revenues increased 5.7% to $33.9 million in the fourth quarter of 2024 compared to $32.1 million in the year ago period, primarily due to a 10.6% ...
Choose from Child Hearing stock illustrations from iStock. Find high-quality royalty-free vector images that you won't find anywhere else. Video Back Videos home Signature collection Essentials ...
Choose from Hearing Disability stock illustrations from iStock. Find high-quality royalty-free vector images that you won't find anywhere else. Video Back Videos home Signature collection Essentials ...
Ten children who received DB-OTO for profound genetic hearing loss due to variants of the otoferlin gene showed notable ...
Learn about the causes of age-related hearing loss and discover effective strategies to manage presbycusis. Early ...
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