Genetics and Auditory Disorders
Seiten
2010
|
Softcover reprint of the original 1st ed. 2002
Springer-Verlag New York Inc.
978-1-4419-3129-0 (ISBN)
Springer-Verlag New York Inc.
978-1-4419-3129-0 (ISBN)
Genetics is fundamental to hearing function, and an understanding of genetics enhances both auditory research and the clinical treatment of the hearing impaired. As a comprehensive review of the genetics of hearing, this book will interest hearing researchers, clinicians and genetic counselors.
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.
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.
and Overview: Genetics in Auditory Science and Clinical Audiology.- Genes and Mutations in Hearing Impairment.- Mapping and Cloning of Genes for Inherited Hearing Impairment.- Genetic Epidemiology of Deafness.- Cytogenetics and Cochlear Expressed Sequence Tags (ESTs) for Identification of Genes Involved in Hearing and Deafness.- Autosomal and X-Linked Auditory Disorders.- Hearing Loss and Mitochondrial DNA Mutations: Clinical Implications and Biological Lessons.- Mice as Models for Human Hereditary Deafness.- Genetic Counseling for Deafness.
| Erscheint lt. Verlag | 6.12.2010 |
|---|---|
| Reihe/Serie | Springer Handbook of Auditory Research ; 14 |
| Zusatzinfo | XII, 324 p. |
| Verlagsort | New York, NY |
| Sprache | englisch |
| Maße | 155 x 235 mm |
| Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete ► HNO-Heilkunde |
| Medizin / Pharmazie ► Medizinische Fachgebiete ► Neurologie | |
| Studium ► 1. Studienabschnitt (Vorklinik) ► Physiologie | |
| Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik | |
| Naturwissenschaften ► Biologie ► Humanbiologie | |
| Naturwissenschaften ► Biologie ► Zoologie | |
| ISBN-10 | 1-4419-3129-5 / 1441931295 |
| ISBN-13 | 978-1-4419-3129-0 / 9781441931290 |
| Zustand | Neuware |
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