Hereditary hearing loss in humans: the importance of genetic approaches for clinical medicine and basic science-Reference-Cited by-同舟云学术

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Hereditary hearing loss in humans: the importance of genetic approaches for clinical medicine and basic science

Published:2014-09 Issue:3 Volume:5 Page:67-71
ISSN:1868-856X
Container-title:e-Neuroforum
language:en
Short-container-title:e-Neuroforum

Author:

Kubisch C.

Publisher

Walter de Gruyter GmbH

Link

http://link.springer.com/content/pdf/10.1007/s13295-014-0061-9

Reference28 articles.

1. Morton CC, Nance WE (2006) Newborn hearing screening-a silent revolution. N Engl J Med 354:2151–2164

2. Davis AC (1989) The prevalence of hearing impairment and reported hearing disability among adults in Great Britain. Int J Epidemiol 18:911–917

3. Noben-Trauth K, Zheng QY, Johnson KR (2003) Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss. Nat Genet 35:21–23

4. Toriello HV, Smith SD (eds) (2013) Hereditary hearing loss and its syndromes (Oxford monographs on medical genetics), 3rd edn. Oxford University Press, Oxford

5. Wang Q, Xue Y, Zhang Y et al (2013) Genetic basis of Y-linked hearing impairment. Am J Hum Genet 92:301–306

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