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Genetics and Auditory Disorders: 14 (Springer Handbook of Auditory Research) - Tapa blanda

 
9781441931290: Genetics and Auditory Disorders: 14 (Springer Handbook of Auditory Research)

Sinopsis

This volume covers gene expression, mutations responsible for various forms of hearing loss, mapping and cloning, as well as mitochondrial and cellular genetics. The authors discuss the fundamentals of genetics so that the reader has a complete understanding of methods used in molecular genetic studies for hearing research. Chapters are also included on the uses of mouse models, genetic epidemiology and genetic counseling specifically for hearing disorders

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Críticas

From the reviews:

"This handbook represents one of the more recent additions to the expanding list of contributions arising from Springer, illuminating progress in auditory research. ... this is an excellent and authoritative description of the state of the art in human auditory genetics. This area is moving so fast and, hence I recommend interested readers to get it now ... ." (R. C. Trembath, Human Genetics, Vol. 114 (3), 2004)

Reseña del editor

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.

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