Pseudohypoaldosteronism type 2: CUL3 mutation confirmed 15 years following initial diagnosis
Intern Med J
.
2022 Apr;52(4):691-692.
doi: 10.1111/imj.15740.
Authors
Bobby Li
1
2
,
Steven Soule
3
,
Thomas Wilkinson
3
,
Chris Florkowski
1
2
Affiliations
1
Canterbury Health Laboratories, Christchurch, New Zealand.
2
Department of Pathology, University of Otago, Christchurch, New Zealand.
3
Department of Endocrinology, Canterbury District Health Board, Christchurch, New Zealand.
PMID:
35419964
DOI:
10.1111/imj.15740
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Cullin Proteins / genetics
Female
Humans
Mutation
Pseudohypoaldosteronism* / diagnosis
Pseudohypoaldosteronism* / genetics
Substances
CUL3 protein, human
Cullin Proteins