Lysosomal Storage Disease upon Disruption of the Neuronal Chloride Transport Protein CIC-6
Lysosomal Storage Disease upon Disruption of the Neuronal Chloride Transport Protein CIC-6
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Washington: National Academy of Sciences
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Language
English
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Publisher
Washington: National Academy of Sciences
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Contents
Mammalian CLC proteins function as Cl⁻ channels or as electrogenic$Cl^{-}/H^{+}$exchangers and are present in the plasma membrane and intracellular vesicles. We now show that the ClC-6 protein is almost exclusively expressed in neurons of the central and peripheral nervous systems, with a particularly high expression in dorsal root ganglia. ClC-6 c...
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Full title
Lysosomal Storage Disease upon Disruption of the Neuronal Chloride Transport Protein CIC-6
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TN_cdi_proquest_journals_201347761
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_201347761
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ISSN
0027-8424
E-ISSN
1091-6490
DOI
10.1073/pnas.0606137103
