MYO15A splicing mutations in hearing loss: A review literature and report of a novel mutation.
Sign Up to like & getrecommendations! Published in 2017 at "International journal of pediatric otorhinolaryngology"
DOI: 10.1016/j.ijporl.2017.03.008
Abstract: Sensorineural hearing loss (SNHL) is the most prevalent genetic sensory defect in humans, affecting about 1 in 1000 newborns around the world. Non-syndromic SNHL accounts for nearly 70% of hereditary hearing loss and 80% of… read more here.
Keywords: hearing loss; mutations hearing; myo15a splicing; splicing mutations ... See more keywords