QuickView for COCH-5B2 (gene)

1. Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.
2. A Novel COCH p.D544Vfs*3 Variant Associated with DFNA9 Sensorineural Hearing Loss Causes Pathologica…
3. In vivo quantification of cochlin in glaucomatous DBA/2J mice using optical coherence tomography.
4. Rational design of a genomically humanized mouse model for dominantly inherited hearing loss, DFNA9.
5. Cochlin in autoimmune inner ear disease: is the search for an inner ear autoantigen over?

There were no clinical trials for COCH-5B2