Results 131 to 134 of about 675 (134)

Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran

International Journal of Pediatric Otorhinolaryngology, 2014
Mortaza Bonyadi, Níkou Fotouhi
exaly  

Case report: Novel GJB2 variant c.113T>C associated with autosomal recessive non-syndromic hearing loss (ARNSHL) in a Han family

Medicine (United States), 2019
exaly  

Autosomal recessive non-syndromic hearing loss is caused by novel compound heterozygous mutations in TMC1 from a Tibetan Chinese family

International Journal of Pediatric Otorhinolaryngology, 2014
exaly  

Expanding the LOXHD1 Mutational Spectrum: A North Indian Case of ARNSHL

Annals of Human Genetics
exaly