Genetic etiology of non-syndromic hearing loss in Latin America
Article in Human Genetics (October 2021)
The most recent citing publications are shown below. View all 10 publications that cite this research output on Dimensions.
Increased prevalence of TG and TPO mutations in Sudanese children with congenital hypothyroidism
Article in The Journal of Clinical Endocrinology & Metabolism (December 2019)
Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects
Article in BMC Medical Genomics (May 2018)