Author:
Fuller Peter J.,Rogerson Fraser M.
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Reference19 articles.
1. Compound heterozygous mutations in the γsubunit gene of ENaC (1627delG and 1570-1G→A) in one sporadic Japanese patient with a systemic form of pseudohypoaldosteronism type 1;Adachi;Journal of Clinical Endocrinology and Metabolism,2000
2. Erthyrocyte Na+,K+-ATPase and nasal potential in pseudohypoaldosteronism;Bistritzer;Clinical Endocrinology,2002
3. Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1;Chang;Nature Genetics,1996
4. A salt-wasting syndrome in infancy;Cheek;Archives of Disease in Childhood,1958
5. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type 1;Geller;Nature Genetics,1998
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