Kobayashi Y, Watanabe T, Hatori M, Matuo Y, Morikawa A, Shimizu N. Two Cases of Sotos Syndrome With Urinary Anomalies and Deletions of Entire NSD1 Gene. Pediatr Nephrol. 2006. 21. 1350
Kobayashi Y, Watanabe T, Hatori M, Matuo Y, Morikawa A, Shimizu N. Two Cases of Sotos Syndrome With Urinary Anomalies and Deletions of Entire NSD1 Gene. Pediatr Nephrol. 2006. 21. 1350
A case of congenital nephrotic syndrome carrying a novel mutation of the NPHS1 gene
(11th Asian Congress of Pediatric Nephrology 2011)
Genome wide analysis of DNA methylation in monocytes and naive T helper cells in minimal change nephrotic syndrome
(11th Asian Congress of Pediatric Nephrology 2011)
