Chloride channels cough up
- 1 October 1997
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 17 (2) , 125-127
- https://doi.org/10.1038/ng1097-125
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type IIINature Genetics, 1997
- A Familial Syndrome of Hypocalcemia with Hypercalciuria Due to Mutations in the Calcium-Sensing ReceptorNew England Journal of Medicine, 1996
- Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridizationNature Genetics, 1996
- A common molecular basis for three inherited kidney stone diseasesNature, 1996
- Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporterNature Genetics, 1996
- A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic ricketsNature Genetics, 1995
- Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidusNature, 1992
- Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytesNature, 1990
- The strychnine-binding subunit of the glycine receptor shows homology with nicotinic acetylcholine receptorsNature, 1987
- Sequence and functional expression of the GABAA receptor shows a ligand-gated receptor super-familyNature, 1987