Author:
Yamada Akio,Usui Kiyotaka,Nagano Yosiko,Shibata Motohiro,Tsuzuki Kazuo
Publisher
Japanese Society for Pediatric Nephrology
Subject
Literature and Literary Theory,History,Cultural Studies
Reference10 articles.
1. 1) Senior B, et al.: Juvenile familial nephropaty with tapetoretinal degeneration. A new oculo-renal dystropy. Am J. Ophthalomol, 52: 625-633, 1961.
2. 2) Smith C, et al.: Congental medullary cysts of the kidneys with severe refractory anemia. Am J Dis Child, 69: 369-377, 1945.
3. 3) Fanconi G, et al.: Familial, juvenile nephronophthisis (idiopathic parenchymal contracted kidney). Helv paediatr Acta, 6: 1-45, 1951.
4. A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1
5. Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
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1 articles.
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1. 10.3165/jjpn.21.167;Nihon Shoni Jinzobyo Gakkai Zasshi;2008