𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Methyl deficiency causes reduction of the methyl-CpG-binding protein, MeCP2, in rat liver

✍ Scribed by Esfandiari, F.


Book ID
119940996
Publisher
Oxford University Press
Year
2003
Tongue
English
Weight
240 KB
Volume
24
Category
Article
ISSN
0143-3334

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Mutations and polymorphisms in the human
✍ Gabriel Miltenberger-Miltenyi; Franco Laccone πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 188 KB

Rett syndrome (RTT or RS) is a neurodevelopmental disorder and one of the most frequent genetic diseases in girls. Mutations of the MECP2 gene have been found in a variety of different RTT phenotypes. The MECP2 gene (Xq28) has been described in 1992. Up to now, 218 different mutations have been repo