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TY  - GEN
AU  - Fraser, G.R.
TI  - Causes of Profound Deafness in Childhood
PY  - 1976///
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TY  - JOUR
AU  - Kelsell, D.P.
TI  - Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
JO  - Nature
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TY  - JOUR
AU  - Steel, K.P.
AU  - Brown, S.D.M.
TI  - Genetics of deafness
JO  - Curr. Opin. in Neurobiol.
PY  - 1996///
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TY  - JOUR
AU  - Guilford, P.
TI  - A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh1 gene
JO  - Hum. Mol. Genet.
PY  - 1994///
VL  - 3
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TY  - JOUR
AU  - Gibson, F.
TI  - A type VII myosin encoded by the mouse deafness gene shaker-1
JO  - Nature
PY  - 1995///
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UR  - http://dx.doi.org/10.1038/374062a0
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TY  - JOUR
AU  - Weil, D.
TI  - Defective myosin VIIA gene responsible for Usher syndrome type 1B
JO  - Nature
PY  - 1995///
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TY  - JOUR
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TI  - Human Usher Ib/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells
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TY  - JOUR
AU  - Liu, X.Z.
AU  - Xu, L.R.
AU  - Zhang, S.L.
AU  - Xu, Y.
TI  - Epidemiological and genetic studies of congenital profound deafness
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PY  - 1992///
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AU  - Stephens, D.
AU  - Francis, M.
TI  - Genetics and Hearing Impairment
PY  - 1996///
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AU  - Weston, M.D.
TI  - Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients
JO  - Am. J. Hum. Genet.
PY  - 1996///
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AU  - Cope, M.J.T.V.
AU  - Whisstock, J.
AU  - Rayment, I.
AU  - Kendrick-Jones, J.
TI  - Conservation within the myosin motor domain: implications for structure and function
JO  - Structure
PY  - 1996///
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AU  - Solc, C.K.
AU  - Derfler, B.H.
AU  - Duyk, G.
AU  - Corey, D.P.
TI  - Molecular cloning of myosins from the bullfrog saccular macula: A candidate for the adaptation motor
JO  - Neurosci.
PY  - 1994///
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AU  - Rayment, I.
TI  - Three-dimensional structure of a myosin subfragment-1: A molecular motor
JO  - Science
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TY  - JOUR
AU  - Liu, X.Z.
AU  - Newton, V.E.
AU  - Steel, K.P.
AU  - Brown, S.D.M.
TI  - Identification of a new mutation of the head region of myosin VII gene in Usher syndrome type 1
JO  - Hum. Mutat.
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TY  - JOUR
AU  - Levy, G.
TI  - Myosin VIIA gene: Heterogeneity of the mutations responsible for Usher syndrome type IB
JO  - Hum. Mol. Genet.
PY  - 1997///
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UR  - http://dx.doi.org/10.1093/hmg/6.1.111
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TY  - JOUR
AU  - Chen, Z.Y.
TI  - Molecular cloning and domain structure of human myosin Vila, the gene product defective in Usher syndrome 1 B
JO  - Genomics
PY  - 1996///
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UR  - http://dx.doi.org/10.1006/geno.1996.0489
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TY  - JOUR
AU  - Liu, X.Z.
AU  - Xu, L.R.
TI  - Non-syndromic genetic deafness: An analysis of audiograms
JO  - Ann. Otol. Rhinol. Laryngol.
PY  - 1994///
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