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Oncotarget , 7 (36), 5840558417
Liddle syndrome has low morbidity and uncommon clinical symptoms, and the diagnosis can only be confirmed by genetic diagnosis, which makes clinical studies of Liddle syndrome more difficult to conduct
Identifying imbalances in these markers allows for targeted medical and lifestyle interventions that can enhance the effectiveness of peptide therapy while reducing the risk of adverse responses
CanaleABenelliGCastagnaASgherriCPoliPSerraAet al
