Population
Five pedigrees (four Australian, one South American) with Familial hyperaldosteronism type II (FH-II).
Design
Other
Authors
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Refines the 7p22 locus in familial hyperaldosteronism type II; leaves open causal variant identification and clinical translation.
This study provides further evidence for the genetic linkage of familial hyperaldosteronism type II to chromosome 7p22, refines the locus, and suggests genetic heterogeneity.
So et al. (2005) studied this question.
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