𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A polymorphic marker in the first intron of the Werner gene associates with cognitive function in aged Danish twins

✍ Scribed by Mette H Bendixen; Bjørn A Nexø; Vilhelm A Bohr; Henrik Frederiksen; Matt McGue; Steen Kølvraa; Kaare Christensen


Book ID
113614494
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
115 KB
Volume
39
Category
Article
ISSN
0531-5565

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Association of a polymorphic variant of
✍ Ye, Lin; Miki, Tetsuro; Nakura, Jun; Oshima, Junko; Kamino, Kouzin; Rakugi, Hiro 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 594 KB

The Werner syndrome (WS) is a rare autosomal recessive progeroid syndrome characterized by the premature onset of multiple age-related disorders, including atherosclerosis, cancer, non-insulin-dependent diabetes mellitus (NIDDM), ocular cataracts and osteoporosis [Epstein et al., 1966]. The major ca