Associated Papers
Focal segmental glomerulosclerosis and neurogenic bladder in a Chinese patient with a novel de novo pathogenic variation in TRIM8 gene: A case report.
Luo DY et al.
Sage Open Medical Case Reports, 2024
Two Children With Steroid-Resistant Significant Proteinuria Due to Nonsense Mutations of the TRIM8 Gene: A Case Report and Literature Review.
Li X et al.
Frontiers in Pediatrics, 2022
Further delineation of the clinical spectrum of de novo TRIM8 truncating mutations.
Assoum M et al.
American Journal of Medical Genetics. Part A, 2018
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