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Two Children With Steroid-Resistant Significant Proteinuria Due to Nonsense Mutations of the TRIM8 Gene: A Case Report and Literature Review

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BackgroundTRIM8 gene mutations have been reported as the genetic basis of autosomal dominant (AD) neuro-renal syndrome in children. which presents with epileptic encephalopathy. focal segmental glomerulosclerosis (FSGS). developmental delay. https://www.fitnessgravesyardes.shop/product-category/heart-rate-grip/
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