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)
The most recent citing publications are shown below. View all 10 publications that cite this research output on Dimensions.
Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss
Article in Frontiers in Genetics (May 2022)
Mutations in LOXHD1 gene can cause auditory neuropathy spectrum disorder
Article in Otolaryngology Case Reports (October 2021)