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Fuchs dystrophy, also referred to as Fuchs endothelial corneal dystrophy (FECD) and Fuchs endothelial dystrophy (FED), is a slowly progressing corneal dystrophy that usually affects both eyes and is slightly more common in women than in men. Although early signs of Fuchs dystrophy are sometimes seen in people in their 30s and 40s, the disease ...
The online video game platform and game creation system Roblox has numerous games (officially referred to as "experiences") [1] [2] created by users of its creation tool, Roblox Studio. Due to Roblox ' s popularity, various games created on the site have grown in popularity, with some games having millions of monthly active players and 5,000 ...
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Here are links to possibly useful sources of information about Fuchs' dystrophy. PubMed provides review articles from the past five years (limit to free review articles) The TRIP database provides clinical publications about evidence-based medicine. Other potential sources include: Centre for Reviews and Dissemination and CDC
This is a list of disorder codes in the Online Mendelian Inheritance in Man (OMIM) database. These are diseases that can be inherited via a Mendelian genetic mechanism. OMIM is one of the databases housed in the U.S. National Center for Biotechnology Information.
A. Aarskog–Scott syndrome; Aase syndrome; Abdallat–Davis–Farrage syndrome; Abruzzo–Erickson syndrome; Achard–Thiers syndrome; Adams–Nance syndrome
Fuchs Petrolub, the world's largest independent manufacturer of lubricants, and related speciality products. Fuchs Group, spice company based in Germany; Fuchs Systems Inc., a German manufacturer of equipment for making steel
329941 Ensembl ENSG00000171812 ENSMUSG00000056174 UniProt P25067 Q4VAQ0 P25318 RefSeq (mRNA) NM_001294347 NM_005202 NM_199473 RefSeq (protein) NP_001281276 NP_005193 NP_955767 Location (UCSC) Chr 1: 36.1 – 36.13 Mb Chr 4: 126.18 – 126.21 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Collagen alpha-2(VIII) chain is a protein that in humans is encoded by the COL8A2 gene ...