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Liddles syndrome: heritable human hypertension caused by mutations in the subunit of the epithelial sodium channel

And a substantial amount of positive data is coming in

Rarity of encephalopathy associated with autoimmune thyroiditis: A case series from Mayo Clinic from 1950 to 1996

Longevity in untreated congenital growth hormone deficiency due to a homozygous mutation in the GHRH receptor gene

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