Liddle Syndrome: Genetics and Mechanisms of Na+ Channel Defects
- 1 December 2001
- journal article
- review article
- Published by Elsevier in The Lancet Healthy Longevity
- Vol. 322 (6) , 302-307
- https://doi.org/10.1097/00000441-200112000-00002
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Association of hypertension with T594M mutation in β subunit of epithelial sodium channels in black people resident in LondonThe Lancet, 1998
- Liddle syndrome: An autosomal dominant form of human hypertensionKidney International, 1998
- Liddle disease caused by a missense mutation of beta subunit of the epithelial sodium channel gene.Journal of Clinical Investigation, 1996
- Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channelCell, 1995
- Role of the actin cytoskeleton on epithelial Na+ channel regulationKidney International, 1995
- Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndromeNature Genetics, 1995
- Liddle's syndrome: A public health menace?American Journal of Kidney Diseases, 1995
- Liddle's syndrome, an underrecognized entity: A report of four cases, including the first report in black individualsAmerican Journal of Kidney Diseases, 1995
- A transmembrane domain of the putative channel subunit MEC-4 influences mechanotransduction and neurodegeneration in C. elegansNature, 1994
- The mec-4 gene is a member of a family of Caenorhabditis elegans genes that can mutate to induce neuronal degenerationNature, 1991