✦ LIBER ✦

Screening for NDP Mutations in 44 Unrelated Patients with Familial Exudative Vitreoretinopathy or Norrie Disease

✍ Scribed by Yang, Huiqin; Li, Shiqiang; Xiao, Xueshan; Guo, Xiangming; Zhang, Qingjiong

Book ID: 119960860
Publisher: Informa plc
Year: 2012
Tongue: English
Weight: 634 KB
Volume: 37
Category: Article
ISSN: 6854-1423
DOI: 10.3109/02713683.2012.675615

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A mutation in the Norrie disease gene (N

A mutation in the Norrie disease gene (NDP) associated with X–linked familial exudative vitreoretinopathy

✍ Chen, Z-Y.; Battinelli, E.M.; Fielder, A.; Bundey, S.; Sims, K.; Breakefield, X. 📂 Article 📅 1993 🏛 Nature Publishing Group 🌐 English ⚖ 436 KB

Overview of the mutation spectrum in fam

Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP

✍ Konstantinos Nikopoulos; Hanka Venselaar; Rob W.J. Collin; Rosa Riveiro-Alvarez; 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 323 KB

Wnt signaling is a crucial component of the cell machinery orchestrating a series of physiological processes such as cell survival, proliferation, and migration. Among the plethora of roles that Wnt signaling plays, its canonical branch regulates eye organogenesis and angiogenesis. Mutations in the