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1. A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment.

Author

del Castillo FJ, Rodríguez-Ballesteros M, Alvarez A, Hutchin T, Leonardi E, de Oliveira CA, Azaiez H, Brownstein Z, Avenarius MR, Marlin S, Pandya A, Shahin H, Siemering KR, Weil D, Wuyts W, Aguirre LA, Martín Y, Moreno-Pelayo MA, Villamar M, Avraham KB, Dahl HH, Kanaan M, Nance WE, Petit C, Smith RJ, Van Camp G, Sartorato EL, Murgia A, Moreno F, and del Castillo I

Subjects
Australia epidemiology, Base Sequence genetics, Belgium epidemiology, Brazil epidemiology, Connexin 26, Connexin 30, DNA Mutational Analysis, Founder Effect, France epidemiology, Gene Frequency, Haplotypes, Hearing Loss epidemiology, Humans, Israel epidemiology, Italy epidemiology, Spain epidemiology, United Kingdom epidemiology, United States epidemiology, Connexins genetics, Hearing Loss genetics, Mutation, Sequence Deletion
Published
2005
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