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000779970 0247_ $$a10.1007/978-3-319-43287-8$$2doi
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000779970 24504 $$aThe role of pendrin in health and disease :$$bmolecular and functional aspects of the SLC26A4 anion exchanger /$$cSilvia Dossena, Markus Paulmichl, editors.
000779970 264_1 $$aCham, Switzerland :$$bSpringer,$$c2017.
000779970 300__ $$a1 online resource (x, 226 pages) :$$billustrations (some color)
000779970 336__ $$atext$$btxt$$2rdacontent
000779970 337__ $$acomputer$$bc$$2rdamedia
000779970 338__ $$aonline resource$$bcr$$2rdacarrier
000779970 347__ $$atext file$$bPDF$$2rda
000779970 500__ $$aIncludes index.
000779970 506__ $$aAccess limited to authorized users.
000779970 520__ $$aThis book reviews the current state of knowledge on the genetics, molecular biology and physiology of pendrin, with a particular focus on pendrin dysfunction and the consequences for human health. Pendrin is a membrane transport protein expressed in the thyroid, inner ear, kidney and airways, and was recently found in a variety of other tissues and organs. Pendrin malfunction may cause a genetic disease called Pendred syndrome or non-syndromic deafness. The book provides a thorough description of the multifaceted role of pendrin in human health and disease. As such, it offers an invaluable tool for physiology and pathology researchers, while also providing essential guidance for otorhinolaryngologists and endocrinologists in the diagnosis of Pendred syndrome and pendrin-related deafness.
000779970 588__ $$aOnline resource; title from PDF title page (SpringerLink, viewed March 9, 2017).
000779970 650_0 $$aMembrane proteins.
000779970 650_0 $$aCell membranes.
000779970 7001_ $$aDossena, Silvia,$$eeditor.
000779970 7001_ $$aPaulmichl, Markus,$$eeditor.
000779970 77608 $$iPrint version:$$z9783319432854$$z3319432850$$w(OCoLC)952981282
000779970 852__ $$bebk
000779970 85640 $$3SpringerLink$$uhttps://univsouthin.idm.oclc.org/login?url=http://link.springer.com/10.1007/978-3-319-43287-8$$zOnline Access$$91397441.1
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