𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Association of a 5178C→A (Leu237Met) polymorphism in the mitochondrial DNA with a low prevalence of myocardial infarction in Japanese individuals

✍ Scribed by Katsumasa Takagi; Yoshiji Yamada; Jian-Sheng Gong; Takahito Sone; Mitsuhiro Yokota; Masashi Tanaka


Book ID
118420336
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
201 KB
Volume
175
Category
Article
ISSN
0021-9150

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