Integration of Human and Mouse Genetics Reveals Pendrin Function in Hearing and Deafness
Author:
Publisher
S. Karger AG
Subject
Physiology
Reference55 articles.
1. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
2. Coupling Modes and Stoichiometry of Cl−/HCO3− Exchange by slc26a3 and slc26a6
3. The Slc26a4 transporter functions as an electroneutral Cl−/I−/HCO3−exchanger: role of Slc26a4 and Slc26a6 in I−and HCO3−secretion and in regulation of CFTR in the parotid duct
4. Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
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