A New Locus on Chromosome 12p13.3 for Pseudohypoaldosteronism Type II, an Autosomal Dominant Form of Hypertension
The American Journal of Human Genetics2000Vol. 67(2), pp. 302–310
Citations Over TimeTop 10% of 2000 papers
Sandra Disse-Nicodème, Jean‐Michel Achard, Isabelle Desitter, Anne-Marie Houot, Albert Fournier, Pierre Corvol, Xavier Jeunemaı̂tre
Related Papers
- → Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance(2018)22 cited
- Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysis.(1990)
- Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.(1988)
- → Molecular pathogenesis of renal pseudohypoaldosteronism type 1(2007)2 cited
- → No evidence of linkage between the locus for autosomal dominant retinitis pigmentosa and D3S47 (C17) in three Australian families(1991)8 cited