Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance

[1] Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : 813 - 821

[2] THE MOUSE SNELLS WALTZER DEAFNESS GENE ENCODES AN UNCONVENTIONAL MYOSIN REQUIRED FOR STRUCTURAL INTEGRITY OF INNER-EAR HAIR-CELLS [J]. NATURE GENETICS, 1995, 11 (04) : 369 - 375

[3] Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (03) : 786 - 793

[4] Chen A, 1997, AM J MED GENET, V71, P467, DOI 10.1002/(SICI)1096-8628(19970905)71:4<467::AID-AJMG18>3.0.CO

[5] 2-E

[6] PHYLOGENETIC ANALYSIS OF THE MYOSIN SUPERFAMILY [J]. CELL MOTILITY AND THE CYTOSKELETON, 1993, 24 (04): : 215 - 223

[7] Mapping of unconventional myosins in mouse and human [J]. GENOMICS, 1996, 36 (03) : 431 - 439

[8] Refined mapping of the usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region [J]. GENOMICS, 1996, 38 (03) : 255 - 263

[9] Mutations in the myosin VIIA gene cause non-syndromic recessive deafness [J]. NATURE GENETICS, 1997, 16 (02) : 188 - 190

[10] Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene [J]. NATURE GENETICS, 1997, 17 (03) : 268 - 269

[1] Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : 813 - 821

[2] THE MOUSE SNELLS WALTZER DEAFNESS GENE ENCODES AN UNCONVENTIONAL MYOSIN REQUIRED FOR STRUCTURAL INTEGRITY OF INNER-EAR HAIR-CELLS [J]. NATURE GENETICS, 1995, 11 (04) : 369 - 375

[3] Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (03) : 786 - 793

[4] Chen A, 1997, AM J MED GENET, V71, P467, DOI 10.1002/(SICI)1096-8628(19970905)71:4<467::AID-AJMG18>3.0.CO

[5] 2-E

[6] PHYLOGENETIC ANALYSIS OF THE MYOSIN SUPERFAMILY [J]. CELL MOTILITY AND THE CYTOSKELETON, 1993, 24 (04): : 215 - 223

[7] Mapping of unconventional myosins in mouse and human [J]. GENOMICS, 1996, 36 (03) : 431 - 439

[8] Refined mapping of the usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region [J]. GENOMICS, 1996, 38 (03) : 255 - 263

[9] Mutations in the myosin VIIA gene cause non-syndromic recessive deafness [J]. NATURE GENETICS, 1997, 16 (02) : 188 - 190

[10] Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene [J]. NATURE GENETICS, 1997, 17 (03) : 268 - 269