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The Role of Pendrin in Health and Disease
Molecular and Functional Aspects of the SLC26A4 Anion Exchanger
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.
This is a digital product.
The Role of Pendrin in Health and Disease: Molecular and Functional Aspects of the SLC26A4 Anion Exchanger and published by Springer. The Digital and eTextbook ISBNs for The Role of Pendrin in Health and Disease are 9783319432878, 3319432877 and the print ISBNs are 9783319432854, 3319432850.
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