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    Respiratory chain deficiency presenting as congenital nephrotic syndrome

    Nephrotic syndrome (NS) in infancy includes NS of Finnish type (mutation of the nephrin gene), diffuse mesangial sclerosis (idiopathic or linked to WT1 mutation), idiopathic NS, most often steroid resistant, and ...

    Alice Goldenberg, Linh Huynh Ngoc, Marie-Christine Thouret… in Pediatric Nephrology (2005)