Artigo Acesso aberto Revisado por pares

A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness ( dn ) locus

1995; Oxford University Press; Volume: 4; Issue: 12 Linguagem: Inglês

10.1093/hmg/4.12.2391

ISSN

1460-2083

Autores

Pawan Kumar Jain, Kunihiro Fukushima, Dilip Deshmukh, Arabandi Ramesh, Elizabeth R. Thomas, Anil K. Lalwani, Subrinder Kumar, Barbara Ploplis, H Skarka, C. R. Srikumari Srisailapathy, Sigrid Wayne, Ross I. S. Zbar, Ishwar C. Verma, Richard J. Smith, Edward R. Wilcox,

Tópico(s)

Cancer-related molecular mechanisms research

Resumo

Journal Article A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus Get access Pawan K. Jain, Pawan K. Jain Laboratory of Molecular Genetics, National Institute on Deafness and other Communication Disorders, National Institutes of HealthRockville, MD 20850-3227 Search for other works by this author on: Oxford Academic PubMed Google Scholar Kunihiro Fukushima, Kunihiro Fukushima 1Molecular Otolaryngology Research Laboratories, Department of Otolaryngology, University of lowalowa City, IA 52242, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Dilip Deshmukh, Dilip Deshmukh 2Rotary Deaf School, Ichalkaranji—Tilawani416 115, Dist. Kolhapur, Maharashtra State Search for other works by this author on: Oxford Academic PubMed Google Scholar Arabandi Ramesh, Arabandi Ramesh 3Department of Genetics, University of MadrasMadras Search for other works by this author on: Oxford Academic PubMed Google Scholar Elizabeth Thomas, Elizabeth Thomas 4All India Institute of Medical SciencesAnsari Nagar, New Delhi 110 029, India Search for other works by this author on: Oxford Academic PubMed Google Scholar Anil K. Lalwani, Anil K. Lalwani 5Laboratory of Molecular Otology, Epstein Laboratories533 Parnassus Ave, U490A, San Francisco, CA 94143-0526, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Subrinder Kumar, Subrinder Kumar 4All India Institute of Medical SciencesAnsari Nagar, New Delhi 110 029, India Search for other works by this author on: Oxford Academic PubMed Google Scholar Barbara Ploplis, Barbara Ploplis Laboratory of Molecular Genetics, National Institute on Deafness and other Communication Disorders, National Institutes of HealthRockville, MD 20850-3227 Search for other works by this author on: Oxford Academic PubMed Google Scholar Hana Skarka, Hana Skarka Laboratory of Molecular Genetics, National Institute on Deafness and other Communication Disorders, National Institutes of HealthRockville, MD 20850-3227 Search for other works by this author on: Oxford Academic PubMed Google Scholar C.R.Srikumari Srisailapathy, C.R.Srikumari Srisailapathy 3Department of Genetics, University of MadrasMadras Search for other works by this author on: Oxford Academic PubMed Google Scholar ... Show more Sigrid Wayne, Sigrid Wayne 1Molecular Otolaryngology Research Laboratories, Department of Otolaryngology, University of lowalowa City, IA 52242, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Ross I.S. Zbar, Ross I.S. Zbar 1Molecular Otolaryngology Research Laboratories, Department of Otolaryngology, University of lowalowa City, IA 52242, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Ishwar C. Verma, Ishwar C. Verma 2Rotary Deaf School, Ichalkaranji—Tilawani416 115, Dist. Kolhapur, Maharashtra State Search for other works by this author on: Oxford Academic PubMed Google Scholar Richard J.H. Smith, Richard J.H. Smith 1Molecular Otolaryngology Research Laboratories, Department of Otolaryngology, University of lowalowa City, IA 52242, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Edward R. Wilcox Edward R. Wilcox * Laboratory of Molecular Genetics, National Institute on Deafness and other Communication Disorders, National Institutes of HealthRockville, MD 20850-3227 *To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 4, Issue 12, December 1995, Pages 2391–2394, https://doi.org/10.1093/hmg/4.12.2391 Published: 01 December 1995 Article history Received: 18 August 1995 Revision received: 15 September 1995 Accepted: 15 September 1995 Published: 01 December 1995

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