Identification of a novel PLS1 heterozygous variant causing autosomal dominant nonsyndromic hearing loss
Abstract
Variant data from clinical exome sequencing in patients with congenital non-syndromic deafness, including one deaf patient
Fields of Study & Subjects
Hearing
Cochlea
Tinnitus
Genetics
Genomics and Rare Diseases
Congenital Ear and Nasal Anomalies
Publication details
- Journal / source
- China National GeneBank DataBase
- Publication date
- 1 January 2026
- Language
- EN