Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Abnormalities and NPHS2[original query] |
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NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children. Pediatric nephrology (Berlin, Germany) 2003 May 18 (5): 412-6. Maruyama Kyoko, Iijima Kazumoto, Ikeda Masahiro, Kitamura Akiko, Tsukaguchi Hiroyasu, Yoshiya Kunihiko, Hoshii Sakurako, Wada Naohiro, Uemura Osamu, Satomura Kenichi, Honda Masataka, Yoshikawa Norishi |
Eye involvement in children with primary focal segmental glomerulosclerosis. Pediatric nephrology (Berlin, Germany) 2008 Mar 23 (3): 421-7. Ozaltin Fatih, Heeringa Saskia, Poyraz Ceren Erdogan, Bilginer Yelda, Kadayifcilar Sibel, Besbas Nesrin, Topaloglu Rezan, Ozen Seza, Hildebrandt Friedhelm, Bakkaloglu Ays |
Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome. Frontiers in genetics 2018 9 214. Abid Aiysha, Shahid Saba, Shakoor Madiha, Lanewala Ali A, Hashmi Seema, Khaliq Shaguf |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 25, 2023
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