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Titlebook: Genetics and Auditory Disorders; Bronya J. B. Keats,Richard R. Fay,Arthur N. Popper Book 2002 Springer Science+Business Media New York 200

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發(fā)表于 2025-3-21 19:01:14 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Genetics and Auditory Disorders
編輯Bronya J. B. Keats,Richard R. Fay,Arthur N. Popper
視頻videohttp://file.papertrans.cn/383/382725/382725.mp4
叢書名稱Springer Handbook of Auditory Research
圖書封面Titlebook: Genetics and Auditory Disorders;  Bronya J. B. Keats,Richard R. Fay,Arthur N. Popper Book 2002 Springer Science+Business Media New York 200
描述Genetics is fundamental to hearing function, and an understanding of genetics enhances both auditory research and the clinical treatment of the hearing impaired. Approaches to the diagnosis and treatment of hearing impairment have developed from technological advances in genetic research. This volume covers gene expression, mutations, mapping and cloning, as well as mitochondrial and cellular genetics. Chapters are also included on the uses of mouse models, genetic epidemiology and genetic counseling specifically for hearing impairment. As a comprehensive review of the genetics of hearing, this book will interest hearing researchers, clinicians and genetic counselors.
出版日期Book 2002
關鍵詞DNA; gene expression; genes; genetic research; genetics; hearing
版次1
doihttps://doi.org/10.1007/b97653
isbn_softcover978-1-4419-3129-0
isbn_ebook978-0-387-21853-3Series ISSN 0947-2657 Series E-ISSN 2197-1897
issn_series 0947-2657
copyrightSpringer Science+Business Media New York 2002
The information of publication is updating

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沙發(fā)
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0947-2657 the hearing impaired. Approaches to the diagnosis and treatment of hearing impairment have developed from technological advances in genetic research. This volume covers gene expression, mutations, mapping and cloning, as well as mitochondrial and cellular genetics. Chapters are also included on the
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0947-2657 uses of mouse models, genetic epidemiology and genetic counseling specifically for hearing impairment. As a comprehensive review of the genetics of hearing, this book will interest hearing researchers, clinicians and genetic counselors.978-1-4419-3129-0978-0-387-21853-3Series ISSN 0947-2657 Series E-ISSN 2197-1897
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Autosomal and X-Linked Auditory Disorders,urther characterization of the genes for hearing loss will provide a clearer vision of the structure and function of the auditory system in health and disease. It is hoped that these discoveries will establish a conceptual basis for the rational therapy of hearing loss and deafness.
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https://doi.org/10.1007/978-3-322-98943-7l hearing impairment have resulted in mapping of 30 autosomal dominant, 28 autosomal recessive and 5 X-linked loci for nonsyndromic hearing impairment. Physical mapping and the use of a variety of cloning approaches over the same time period have led to the identification of 18 of these genes. Furth
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