The Role of Pendrin in Health and Disease : Molecular and Functional Aspects of the SLC26A4 Anion Exchanger
Softcover Reprint of the Original 1st 2017 ed.
Book Details
Format
Paperback / Softback
ISBN-10
3319827804
ISBN-13
9783319827803
Edition
Softcover Reprint of the Original 1st 2017 ed.
Publisher
Springer International Publishing AG
Imprint
Springer International Publishing AG
Country of Manufacture
GB
Country of Publication
GB
Publication Date
Jul 20th, 2018
Print length
226 Pages
Product Classification:
Medical researchMedical geneticsEndocrinologyOtorhinolaryngology (ENT)
Ksh 23,400.00
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This book reviews the current state of knowledge on the genetics, molecular biology and physiology of pendrin, with a particular focus on pendrin dysfunction and the consequences for human health.
This book reviews the current state of knowledge on the genetics, molecular biology and physiology of pendrin, with a particular focus on pendrin dysfunction and the consequences for human health. Pendrin is a membrane transport protein expressed in the thyroid, inner ear, kidney and airways, and was recently found in a variety of other tissues and organs. Pendrin malfunction may cause a genetic disease called Pendred syndrome or non-syndromic deafness. The book provides a thorough description of the multifaceted role of pendrin in human health and disease. As such, it offers an invaluable tool for physiology and pathology researchers, while also providing essential guidance for otorhinolaryngologists and endocrinologists in the diagnosis of Pendred syndrome and pendrin-related deafness.
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