✦ LIBER ✦

Coding Variant I62V in the Complement Factor H Gene Is Strongly Associated with Polypoidal Choroidal Vasculopathy

✍ Scribed by Naoshi Kondo; Shigeru Honda; Shin-ichi Kuno; Akira Negi

Book ID: 116805203
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 263 KB
Volume: 116
Category: Article
ISSN: 0161-6420
DOI: 10.1016/j.ophtha.2008.11.011

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Role of Complement Factor H I62V and Age

Role of Complement Factor H I62V and Age-Related Maculopathy Susceptibility 2 A69S Variants in the Clinical Expression of Polypoidal Choroidal Vasculopathy

✍ Yoichi Sakurada; Takeo Kubota; Mitsuhiro Imasawa; Fumihiko Mabuchi; Yasushi Tate 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 246 KB

The Association of Age-related Maculopat

The Association of Age-related Maculopathy Susceptibility 2 (ARMS2) and Complement Factor H (CFH) Variants with Two Angiographic Subtypes of Polypoidal Choroidal Vasculopathy

✍ Miki, Akiko; Honda, Shigeru; Kondo, Naoshi; Negi, Akira 📂 Article 📅 2013 🏛 Informa plc 🌐 English ⚖ 211 KB

A Common Polymorphism in the Complement

A Common Polymorphism in the Complement Factor H Gene Is Associated With Increased Risk of Myocardial Infarction: The Rotterdam Study

✍ Isabella Kardys; Caroline C.W. Klaver; Dominiek D.G. Despriet; Arthur A.B. Berge 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 266 KB

A genetic polymorphism in the coding reg

A genetic polymorphism in the coding region of the gastric intrinsic factor gene (GIF) is associated with congenital intrinsic factor deficiency

✍ Marilyn M. Gordon; Nancy Brada; Angel Remacha; Isabel Badell; Elisabeth del Río; 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 265 KB 👁 1 views

Congenital intrinsic factor (IF) deficiency is a disorder characterized by megaloblastic anemia due to the absence of gastric IF (GIF, GenBank NM \_ 005142) and GIF antibodies, with probable autosomal recessive inheritance. Most of the reported patients are isolated cases without genetic studies of

The Y402H variant of complement factor H

The Y402H variant of complement factor H is associated with age-related macular degeneration but not with diabetic retinal disease in the Go-DARTS study

✍ A. S. F. Doney; G. P. Leese; J. Olson; A. D. Morris; C. N. A. Palmer 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 135 KB

A variant in the transcription factor 7-

A variant in the transcription factor 7-like 2 (TCF7L2) gene is associated with an increased risk of gestational diabetes mellitus

✍ N. Shaat; Å. Lernmark; E. Karlsson; S. Ivarsson; H. Parikh; K. Berntorp; L. Groo 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 170 KB