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Results 1 - 8 of 8 for Pseudohypoaldosteronism type 1 autosomal dominant
  1. ... NR3C2 gene have been identified in people with pseudohypoaldosteronism type 1 (PHA1), a condition that typically begins ... are the principal cause of renal type 1 pseudohypoaldosteronism. Hum Mutat. 2007 Jan;28(1):33-40. ...
  2. ... the WNK4 gene have been found to cause pseudohypoaldosteronism type 2 (PHA2), a condition characterized by high ... of high blood pressure (hypertension) in people without pseudohypoaldosteronism type 2. A combination of genetic variations and ...
  3. ... a dozen mutations in the SCNN1A gene cause pseudohypoaldosteronism type 1 (PHA1). This condition typically begins in ... sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nat Genet. 1996 Mar;12(3): ...
  4. ... KLHL3 gene mutations have been found to cause pseudohypoaldosteronism type 2 (PHA2), a condition characterized by high ...
  5. ... SCNN1B gene have been identified in people with pseudohypoaldosteronism type 1 (PHA1). This condition typically begins in ... sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nat Genet. 1996 Mar;12(3): ...
  6. ... SCNN1G gene are involved in a condition called pseudohypoaldosteronism type 1 (PHA1). This condition typically begins in ... sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nat Genet. 1996 Mar;12(3): ...
  7. ... the WNK1 gene have been found to cause pseudohypoaldosteronism type 2 (PHA2), a condition characterized by high ...
  8. ... particular region of the CUL3 gene can cause pseudohypoaldosteronism type 2 (PHA2), a condition characterized by high ...