Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome

[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] Molecular cloning and domain structure of human myosin-VIIa. The gene product defective in usher syndrome 1B [J]. GENOMICS, 1996, 36 (03) : 440 - 448

[3] Conservation within the myosin motor domain: Implications for structure and function [J]. STRUCTURE, 1996, 4 (08) : 969 - 987

[4] Unconventional myosins, the basis for deafness in mouse and man [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : 801 - 805

[5] Usher syndrome in the city of Birmingham - Prevalence and clinical classification [J]. BRITISH JOURNAL OF OPHTHALMOLOGY, 1997, 81 (01) : 46 - 53

[6] Myosin VIIA gene: Heterogeneity of the mutations responsible for Usher syndrome type IB [J]. HUMAN MOLECULAR GENETICS, 1997, 6 (01) : 111 - 116

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

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

[9] Liu XZ, 1997, HUM MUTAT, V10, P168, DOI 10.1002/(SICI)1098-1004(1997)10:2<168::AID-HUMU10>3.0.CO

[10] 2-Y

[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] Molecular cloning and domain structure of human myosin-VIIa. The gene product defective in usher syndrome 1B [J]. GENOMICS, 1996, 36 (03) : 440 - 448

[3] Conservation within the myosin motor domain: Implications for structure and function [J]. STRUCTURE, 1996, 4 (08) : 969 - 987

[4] Unconventional myosins, the basis for deafness in mouse and man [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : 801 - 805

[5] Usher syndrome in the city of Birmingham - Prevalence and clinical classification [J]. BRITISH JOURNAL OF OPHTHALMOLOGY, 1997, 81 (01) : 46 - 53

[6] Myosin VIIA gene: Heterogeneity of the mutations responsible for Usher syndrome type IB [J]. HUMAN MOLECULAR GENETICS, 1997, 6 (01) : 111 - 116

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

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

[9] Liu XZ, 1997, HUM MUTAT, V10, P168, DOI 10.1002/(SICI)1098-1004(1997)10:2<168::AID-HUMU10>3.0.CO

[10] 2-Y