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However, these changes were not significantly different between them
PMID: 28671236
Pathogenic variants in the SCNN1B and SCNN1G genes are the causes of Liddle syndrome with pathogenic variants in the SCNN1B gene being identified in the individuals in the original pedigree of Liddle syndrome
For acute pain crises, cortisone may still be the pragmatic choice
This personalization can improve outcomes by focusing on what works best for the patient
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