Faculty Opinions recommendation of CLCN2 chloride channel mutations in familial hyperaldosteronism type II.

2018 ◽  
Author(s):  
David Pearce
Keyword(s):  
Chloride Channel ◽  
Type Ii ◽  
Familial Hyperaldosteronism

scholarly journals CLCN2 clicks with aldosterone-producing adenomas, too!

2019 ◽  
Vol 181 (5) ◽  
pp. C21-C22
Author(s):  
Ute I Scholl
Keyword(s):  
Chloride Channel ◽  
Germline Mutations ◽  
Type Ii ◽  
Channel Gene ◽  
Disease Spectrum ◽  
Familial Hyperaldosteronism ◽  
Aldosterone Producing Adenoma

Germline mutations in the chloride channel gene CLCN2 have been described as cause of familial hyperaldosteronism type II. In this issue, Dutta and colleagues in a groundbreaking study identify a somatic (tumor-specific) CLCN2 mutation in an aldosterone-producing adenoma, expanding the disease spectrum associated with CLCN2 mutations.

scholarly journals CLCN2 chloride channel mutations in familial hyperaldosteronism type II

2018 ◽  
Vol 50 (3) ◽  
pp. 349-354 ◽  
Author(s):  
Ute I. Scholl ◽  
Gabriel Stölting ◽  
Julia Schewe ◽  
Anne Thiel ◽  
Hua Tan ◽  
...  
Keyword(s):  
Chloride Channel ◽  
Type Ii ◽  
Familial Hyperaldosteronism

scholarly journals CLCN2 chloride channel mutations in familial hyperaldosteronism type II

2018 ◽  
Author(s):  
Scholl UI ◽  
Stölting G ◽  
Schewe J ◽  
Thiel A ◽  
Tan H ◽  
...  
Keyword(s):  
Chloride Channel ◽  
Type Ii ◽  
Familial Hyperaldosteronism

Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families

2008 ◽  
Vol 26 (8) ◽  
pp. 1577-1582 ◽  
Author(s):  
Norlela Sukor ◽  
Paolo Mulatero ◽  
Richard D Gordon ◽  
Albertina So ◽  
David Duffy ◽  
...  
Keyword(s):  
South American ◽  
Type Ii ◽  
Familial Hyperaldosteronism ◽  
American Families

scholarly journals Familial Hyperaldosteronism Type II: Description of a Large Kindred and Exclusion of the Aldosterone Synthase (CYP11B2) Gene1

1998 ◽  
Vol 83 (9) ◽  
pp. 3214-3218 ◽  
Author(s):  
David J. Torpy ◽  
Richard D. Gordon ◽  
Jing Ping Lin ◽  
Phillip R. Huggard ◽  
Susan E. Taymans ◽  
...  
Keyword(s):  
Type Ii ◽  
Aldosterone Synthase ◽  
Familial Hyperaldosteronism

scholarly journals Further study of chromosome 7p22 to identify the molecular basis of familial hyperaldosteronism type II

2010 ◽  
Vol 25 (9) ◽  
pp. 560-564 ◽  
Author(s):  
K J Carss ◽  
M Stowasser ◽  
R D Gordon ◽  
K M O'Shaughnessy
Keyword(s):  
Molecular Basis ◽  
Type Ii ◽  
Familial Hyperaldosteronism

FAMILIAL HYPERALDOSTERONISM TYPE II (FH-II) IS MORE COMMON THAN TYPE I (FH-I) AND DEMONSTRATES LINKAGE TO CHROMOSOME 7P22

2004 ◽  
Vol 22 (Suppl. 1) ◽  
pp. S165
Author(s):  
M. Stowasser ◽  
R. D. Gordon ◽  
M. S. Elphinstone ◽  
A. So
Keyword(s):  
Type I ◽  
Type Ii ◽  
Familial Hyperaldosteronism
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