Journal article
Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss-loci on human chromosome 9q and mouse chromosome 19
Gene, Vol.215(2), pp.461-469
1998
DOI: 10.1016/S0378-1119(98)00316-3
PMID: 9758550
Abstract
The DFNB7/11 locus for autosomal recessive non-syndromic hearing loss (ARNSHL) has been mapped to an approx. 1.5
Details
- Title: Subtitle
- Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss-loci on human chromosome 9q and mouse chromosome 19
- Creators
- D.A Scott - Department of Pediatrics, University of Iowa Hospitals and Clinics, Iowa City, IA, USAJ.H Greinwald - Molecular Otolaryngology Research Laboratories, Department of Otolaryngology – Head and Neck Surgery, University of Iowa Hospitals and Clinics, Iowa City, IA, USAJ.R Marietta - Molecular Otolaryngology Research Laboratories, Department of Otolaryngology – Head and Neck Surgery, University of Iowa Hospitals and Clinics, Iowa City, IA, USAS Drury - Department of Biometry and Genetics, Louisiana State University Medical Center, New Orleans, LA, USAR.E Swiderski - Department of Pediatrics, University of Iowa Hospitals and Clinics, Iowa City, IA, USAA Viñas - Department of Biochemistry and Molecular Biology, Louisiana State University Medical Center, New Orleans, LA, USAM.M DeAngelis - Department of Biometry and Genetics, Louisiana State University Medical Center, New Orleans, LA, USAR Carmi - Genetics Institute,Soroka Medical Center, Ben Gurion University of Negev, Beer-Sheva, IsraelA Ramesh - Department of Genetics, University of Madras, Madras, IndiaM.L Kraft - Molecular Otolaryngology Research Laboratories, Department of Otolaryngology – Head and Neck Surgery, University of Iowa Hospitals and Clinics, Iowa City, IA, USAK Elbedour - Genetics Institute,Soroka Medical Center, Ben Gurion University of Negev, Beer-Sheva, IsraelA.B Skworak - Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USAR.A Friedman - Department of Otolaryngology – Head and Neck Surgery, University of Cincinnati, Cincinnati, OH, USAC.R Srikumari Srisailapathy - Department of Genetics, University of Madras, Madras, IndiaK Verhoeven - Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, BelgiumG Van Camp - Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, BelgiumM Lovett - Department of University of Texas Southwestern Medical Center, Dallas, TX 75235, USAP.L Deininger - Department of Biochemistry and Molecular Biology, Louisiana State University Medical Center, New Orleans, LA, USAM.A Batzer - Department of Biometry and Genetics, Louisiana State University Medical Center, New Orleans, LA, USAC.C Morton - Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USAB.J Keats - Department of Biometry and Genetics, Louisiana State University Medical Center, New Orleans, LA, USAR.J.H Smith - Molecular Otolaryngology Research Laboratories, Department of Otolaryngology – Head and Neck Surgery, University of Iowa Hospitals and Clinics, Iowa City, IA, USAV.C Sheffield - Department of Pediatrics, University of Iowa Hospitals and Clinics, Iowa City, IA, USA
- Resource Type
- Journal article
- Publication Details
- Gene, Vol.215(2), pp.461-469
- Publisher
- Elsevier B.V
- DOI
- 10.1016/S0378-1119(98)00316-3
- PMID
- 9758550
- ISSN
- 0378-1119
- eISSN
- 1879-0038
- Language
- English
- Date published
- 1998
- 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; Medical Genetics and Genomics; Otolaryngology; Internal Medicine; Ophthalmology and Visual Sciences
- Record Identifier
- 9984006493302771
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