Heterozygous MYH9 Mutations in 2 Children With Cochlear Nerve Canal Stenosis.
Article in Ear, Nose & Throat Journal (October 2022)
The most recent citing publications are shown below. View all 8 publications that cite this research output on Dimensions.
A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options
Article in Clinical Genetics (September 2022)
Genetic etiology of non-syndromic hearing loss in Latin America
Article in Human Genetics (October 2021)