Author:
Robertson Nahid G.,Lu Leonard,Heller Stefan,Merchant Saumil N.,Eavey Roland D.,McKenna Michael,Nadol Joseph B.,Miyamoto Richard T.,Linthicum Frederick H.,Lubianca Neto José F.,Hudspeth A.J.,Seidman Christine E.,Morton Cynthia C.,Seidman J.G.
Publisher
Springer Science and Business Media LLC
Reference29 articles.
1. Cohen, M.M. & Gorlin, R.J. Epidemiology, etiology, and genetic patterns. in Hereditary Hearing Loss and Its Syndromes (eds Gorlin, R.J., Toriello, H.V. & Cohen, M.M.) 9–21 (Oxford University Press, New York, 1995).
2. Petit, C. Genes responsible for human hereditary deafness: symphony of a thousand. Nature Genet. 14, 385–391 (1996).
3. Van Camp, G., Willems, P.J. & Smith, R.J.H. Nonsyndromic hearing impairment: unparalleled heterogeneity. Am. J. Hum. Genet. 60, 758– 764 (1997).
4. Liu, X.-Z. et al. Mutations in the myosin VIIA gene cause nonsyndromic recessive deafness. Nature Genet. 16, 188– 190 (1997).
5. Weil, D. et al. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin VIIA gene. Nature Genet. 16, 191–193 (1997).
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