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Background Familial steroid-sensitive nephrotic syndrome (SSNS) is a rare condition. The disease pathophysiology remains elusive. However, bi-allelic mutations in the EMP2 gene were identified, and specific variations in HLA-DQA1 were linked to a high risk of developing the disease. Methods Clinical data were analyzed in 59 SSNS families. EMP2 gene was sequenced in families with a potential autosomal...
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