Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort

Author:

Carvalho Simone da Costa e SilvaORCID,Grangeiro Carlos Henrique Paiva,Picanço-Albuquerque Clarissa Gondim,dos Anjos Thaís Oliveira,De Molfetta Greice Andreotti,Silva Wilson Araujo,Ferraz Victor Evangelista de Faria

Funder

CNPq

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference28 articles.

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2. Lin F, Li D, Wang P, Fan D, De J, Zhu W. Autosomal recessive non-syndromic hearing loss is caused by novel compound heterozygous mutations in TMC1 from a Tibetan Chinese family. Int J Pediatr Otorhinolaryngol. 2014;78:2216–21.

3. Van Camp G; Smih R. Hereditary hearing loss homepage, nonsyndromic genes, autosomal recessive. In: Hereditary hearing loss homepage; 2017. http://hereditaryhearingloss.org . Accessed 30 July 2017.

4. Najmabadi H, Kahrizi K. Genetics of non-syndromic hearing loss in the Middle East. Int J Pediatr Otorhinolaryngol. 2014;78:2026–36.

5. Sanchez HA, Verselis VK. Aberrant Cx26 hemichannels and keratitis-ichthyosis-deafness syndrome: insights into syndromic hearing loss. Front Cell Neurosci. 2014;8:1–10.

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