Author:
Luo Na,Lu Jingping,Sun Yang
Subject
Sensory Systems,Ophthalmology
Reference55 articles.
1. Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome;Arts;Nature Genetics,2007
2. Pharbin, a novel inositol polyphosphate 5-phosphatase, induces dendritic appearances in fibroblasts;Asano;Biochemical and Biophysical Research Communications,1999
3. The Lowe’s oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase;Attree;Nature,1992
4. Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies;Bielas;Nature Genetics,2009
5. Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome;Cantagrel;American Journal of Human Genetics,2008
Cited by
32 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献