A new locus on chromosome 12p13.3 for Pseudohypoaldosteronism type II, an autosomal dominant form of hypertension

American Journal of Human Genetics

Volumn 67, Issue 2, 2000, Pages 302-310

  Disse Nicodeme, Sandra ^a   Achard, Jean Michel ^c   Desitter, Isabelle ^a   Houot, Anne Marie ^a   Fournier, Albert ^c   Corvol, Pierre ^a,b   Jeunemaitre, Xavier ^a,b  

^a l'alimentation et l'Environnement   (France)

^b HÔPITAL BROUSSAIS   (France)

^c AMIENS UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 12P; CHROMOSOME MAP; CLINICAL ARTICLE; FEMALE; GENE LOCATION; GENE LOCUS; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC MARKER; HUMAN; HYPERCHLOREMIC ACIDOSIS; HYPERKALEMIA; HYPERTENSION; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PSEUDOHYPOALDOSTERONISM;

EID: 0033855576     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/303020     Document Type: Article

References (21)

1. Relationship between blood pressure and weight characteristics in childhood and adolescence
2. Hyperkalemia, hypertension and systemic acidosis without renal failure associated with a tubular defect in potassium excretion
3. Familial hyperkalemia, hypertension, and hyporeninemia with normal aldosterone levels: A tubular defect in potassium handling
4. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
5. Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1
6. Familial hyperpotassemia and hypertension accompanied by normal plasma aldosterone levels: Possible hereditary cell membrane defect
7. Hypertension and severe hyperkalaemia associated with suppression of renin and aldosterone and completely reversed by dietary sodium restriction
8. Gordon's syndrome: A sodium-volume-dependent form of hypertension with a genetic basis
9. Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10
10. Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
11. Molecular genetics of human blood pressure variation
12. Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21
13. Linkage of Gordon's syndrome to the long arm of chromosome 17 in a region recently linked to familial essential hypertension
14. Mineralo corticoid-resistant renal hyperkalemia without salt wasting (type II pseudohypoaldosteronism): Role of increased renal chloride reabsorption
15. Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12
16. Association of a human G-protein beta3 subunit variant with hypertension
17. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
18. WW domains of Nedd4 bind to the prolinerich PY motifs in the epithelial Na+ channel deleted in Liddle's syndrome
19. Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis
20. Guidelines for the management of hypertension. Guidelines subcommittee