Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00439-021-02311-1.pdf
Reference92 articles.
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2. Antonelli PJ, Nall AV, Lemmerling MM, Mancuso AA, Kubilis PS (1998) Hearing loss with cochlear modiolar defects and large vestibular aqueducts. Am J Otol 19:306–312
3. Azaiez H, Yang T, Prasad S, Sorensen JL, Nishimura CJ, Kimberling WJ, Smith RJ (2007) Genotype-phenotype correlations for SLC26A4-related deafness. Hum Genet 122:451–457. https://doi.org/10.1007/s00439-007-0415-2
4. Baldwin CT, Weiss S, Farrer LA, De Stefano AL, Adair R, Franklyn B, Kidd KK, Korostishevsky M, Bonné-Tamir B (1995) Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. Hum Mol Genet 4:1637–1642. https://doi.org/10.1093/hmg/4.9.1637
5. Berrettini S, Forli F, Bogazzi F, Neri E, Salvatori L, Casani AP, Franceschini SS (2005) Large vestibular aqueduct syndrome: audiological, radiological, clinical, and genetic features. Am J Otolaryngol 26:363–371. https://doi.org/10.1016/j.amjoto.2005.02.013
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