Potential treatments for genetic hearing loss in humans: current conundrums
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
http://www.nature.com/articles/gt201527.pdf
Reference52 articles.
1. Morton CC, Nance WE . Newborn hearing screening—a silent revolution. N Engl J Med 2006; 354: 2151–2164.
2. Van Camp G, Willems PJ, Smith RJ . Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet 1997; 60: 758–764.
3. ACMG. Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statement. Genet Med 2002; 4: 162–171.
4. Smith RJ, Bale JF Jr, White KR . Sensorineural hearing loss in children. Lancet 2005; 365: 879–890.
5. Schrijver I . Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound. J Mol Diagn 2004; 6: 275–284.
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