Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration-Reference-Cited by-同舟云学术

Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration

Published:2005-02-10 Issue:5 Volume:24 Page:1079-1091
ISSN:0261-4189
Container-title:The EMBO Journal
language:
Short-container-title:EMBO J

Author:

Kasper Dagmar,Planells-Cases Rosa,Fuhrmann Jens C,Scheel Olaf,Zeitz Oliver,Ruether Klaus,Schmitt Anja,Poët Mallorie,Steinfeld Robert,Schweizer Michaela,Kornak Uwe,Jentsch Thomas J

Publisher

Wiley

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Reference41 articles.

1. Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channels

2. ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family

3. Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive osteopetrosis

4. Albers-Schonberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene

5. Chloride is an allosteric effector of copper assembly for the yeast multicopper oxidase Fet3p: An unexpected role for intracellular chloride channels

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