Novel Pathogenic Variants in the Gene Encoding Stereocilin (STRC) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean Subjects - Domínguez-Ruiz, María; Ruiz-Palmero, Laura; Buonfiglio, Paula I.; García-Vaquero, Irene; Gómez-Rosas, Elena; Goñi, Marina; Villamar, Manuela; Morín, Matías; Moreno-Pelayo, Miguel A.; Elgoyhen, Ana B.; del Castillo, Francisco J.; Dalamón, Viviana; et al. (Biomedicines, 2023)
Keywords: DFNB16; DNA sequencing; Epidemiology; Genes; Genetic aspects; genetic epidemiology; Genetics; Genomes; Genomics; Genotypes; Haplotypes; Hearing loss; Hearing protection; Multiprocessing; Mutation; non-syndromic hearing impairment; Nucleotide sequencing; Phenotypes; Siblings; stereocilin; STRC; Argentina; Spain; United States--US; non-syndromic hearing impairment; DFNB16; STRC; stereocilin; genetic epidemiology