Author:
Watanabe Miki,Nakagawa Ryuji,Kohmoto Tomohiro,Naruto Takuya,Suga Ken-ichi,Goji Aya,Horikawa Hideaki,Masuda Kiyoshi,Kagami Shoji,Imoto Issei
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Biochemistry
Reference15 articles.
1. Loi M . Lowe syndrome. Orphanet J Rare Dis 2006; 1: 16.
2. Lewis RA, Nussbaum RL, Brewer ED. Low syndrome. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH et al. (eds). GeneReviews. University of Washington, Seattle: Seattle, WA, USA, 1993–2016, 2001 July 24 [Updated 2012 February 23].
3. Bökenkamp A, Ludwig M. The oculocerebrorenal syndrome of Lowe: an update. Pediatr Nephrol 2016; e-pub ahead of print 24 March 2016; doi:10.1007/s00467-016-3343-3.
4. Attree O, Olivos IM, Okabe I, Bailey LC, Nelson DL, Lewis RA et al. The Lowe’s oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase. Nature 1992; 358: 239–242.
5. Peces R, Peces C, de Sousa E, Vega C, Selgas R, Nevado J . A novel and de novo deletion in the OCRL1 gene associated with a severe form of Lowe syndrome. Int Urol Nephrol 2013; 45: 1767–1771.
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