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OverviewHearing Impairment is among the most common neurosensory deficit in humans. World wide more than 250 million people suffer from hearing impairment. This high ratio offer more attention to this problem of Human race. With the emergence of Genomics, our understanding towards the hereditary hearing loss has become more extensive. Role of different genes, their molecular organization, function and mutations, giving an insight of disease development. the study of hearing impairment provide a unique opportunity to deal with two objects simultaneously;1) underlying the pathogenic process in each form of deafness and 2) identification of causative genes and cellular mechanism of hearing. Deafness has many Genetic and Environmental causes. Genetic Hearing Impairment can be classified as Syndromic (30%)and Non-Syndromic (70%)genetic defect.More than 50 nuclear genes have been identified associated with Non-Syndromic Hearing impairment. This high degree of genetic heterogeneity reflects the great diversity of specialized proteins that are required to make sense of Sound Full Product DetailsAuthor: Ahmad Farooq , Dr. Wasim AhmadPublisher: VDM Verlag Dr. Muller Aktiengesellschaft & Co. KG Imprint: VDM Verlag Dr. Muller Aktiengesellschaft & Co. KG Dimensions: Width: 15.20cm , Height: 1.00cm , Length: 22.90cm Weight: 0.262kg ISBN: 9783639259926ISBN 10: 3639259920 Pages: 172 Publication Date: 07 September 2011 Audience: General/trade , General Format: Paperback Publisher's Status: Active Availability: In Print  This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us. Table of ContentsReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |
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