- Title: Subtitle
- 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
- Creators
- F J del Castillo - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaM Rodríguez-Ballesteros - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaA Álvarez - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaT Hutchin - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaE Leonardi - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaC A de Oliveira - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaH Azaiez - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaZ Brownstein - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaM R Avenarius - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaS Marlin - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaA Pandya - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaH Shahin - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaK R Siemering - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaD Weil - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaW Wuyts - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaL A Aguirre - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaY Martín - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaM A Moreno-Pelayo - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaM Villamar - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaK B Avraham - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaH-H M Dahl - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaM Kanaan - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaW E Nance - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaC Petit - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaR J H Smith - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaG Van Camp - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaE L Sartorato - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaA Murgia - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaF Moreno - Department of Paediatrics, University of Melbourne, Melbourne, AustraliaI del Castillo - Department of Paediatrics, University of Melbourne, Melbourne, Australia
- Resource Type
- Letter/Communication
- Publication Details
- Journal of medical genetics, Vol.42(7), pp.588-594
- DOI
- 10.1136/jmg.2004.028324
- PMID
- 15994881
- PMCID
- PMC1736094
- NLM abbreviation
- J Med Genet
- ISSN
- 0022-2593
- eISSN
- 1468-6244
- Language
- English
- Date published
- 07/2005
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
- Record Identifier
- 9984006309302771
Letter/Communication
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
Journal of medical genetics, Vol.42(7), pp.588-594
07/2005
DOI: 10.1136/jmg.2004.028324
PMCID: PMC1736094
PMID: 15994881
Details
Metrics
31 Record Views