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Page 1
Mutation analysis of the mouse myosin VIIA deafness gene.
Mburu P, Liu XZ, Walsh J, Saw D Jr, Cope MJ, Gibson F, Kendrick-Jones J, Steel KP, Brown SD. Mburu P, et al. Among authors: walsh j. Genes Funct. 1997 Jun;1(3):191-203. doi: 10.1046/j.1365-4624.1997.00020.x. Genes Funct. 1997. PMID: 9680294
A type VII myosin encoded by the mouse deafness gene shaker-1.
Gibson F, Walsh J, Mburu P, Varela A, Brown KA, Antonio M, Beisel KW, Steel KP, Brown SD. Gibson F, et al. Among authors: walsh j. Nature. 1995 Mar 2;374(6517):62-4. doi: 10.1038/374062a0. Nature. 1995. PMID: 7870172
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD, et al. Weil D, et al. Among authors: walsh j. Nature. 1995 Mar 2;374(6517):60-1. doi: 10.1038/374060a0. Nature. 1995. PMID: 7870171
Unravelling the genetics of deafness.
Steel KP, Mburu P, Gibson F, Walsh J, Varela A, Brown K, Self T, Mahony M, Fleming J, Pearce A, Harvey D, Cable J, Brown SD. Steel KP, et al. Among authors: walsh j. Ann Otol Rhinol Laryngol Suppl. 1997 May;168:59-62. Ann Otol Rhinol Laryngol Suppl. 1997. PMID: 9153119 Review.
Sensorineural hearing impairment non-syndromic, dominant DFNA11.
Tamagawa Y, Kitamura K, Ishida T, Nishizawa M, Liu XZ, Walsh J, Steel KP, Brown SD. Tamagawa Y, et al. Among authors: walsh j. Adv Otorhinolaryngol. 2000;56:103-6. doi: 10.1159/000059092. Adv Otorhinolaryngol. 2000. PMID: 10868221 No abstract available.
5,993 results