𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility

✍ Scribed by Weiss, Lauren A; Kosova, Gülüm; Delahanty, Ryan J; Jiang, Lan; Cook, Edwin H; Ober, Carole; Sutcliffe, James S


Book ID
110026646
Publisher
Nature Publishing Group
Year
2006
Tongue
English
Weight
209 KB
Volume
14
Category
Article
ISSN
1018-4813

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Novel polymorphic AluYb8 insertion in th
✍ Margus Putku; Katrin Kepp; Elin Org; Siim Sõber; David Comas; Margus Viigimaa; G 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 221 KB

Mutations in __WNK1__ and __WNK4__ cause familial hypertension, the Gordon syndrome. __WNK1__ and __WNK4__ conserved noncoding regions were targeted to polymorphism screening using DHPLC and DGGE. The scan identified an undescribed polymorphic __AluYb8__ insertion in __WNK1__ intron 10. Screening in