𝔖 Bobbio Scriptorium
✦   LIBER   ✦

MeCP2 dysfunction in Rett syndrome and related disorders

✍ Scribed by Paolo Moretti; Huda Y Zoghbi

Book ID
116505067
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
135 KB
Volume
16
Category
Article
ISSN
0959-437X

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

MECP2 mutations in Serbian Rett syndrome
MECP2 mutations in Serbian Rett syndrome patients
✍ A. Djarmati; V. DobričiΔ‡; M. KecmanoviΔ‡; P. Marsh; J. JančiΔ‡-StefanoviΔ‡; C. Klei πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 224 KB
MECP2 deletions and genotype–phenotype c
MECP2 deletions and genotype–phenotype correlation in Rett syndrome
✍ Elisa Scala; Ilaria Longo; Federica Ottimo; Caterina Speciale; Katia Sampieri; E πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 184 KB πŸ‘ 2 views

## Abstract Rett syndrome is a neurodevelopmental disorder that represents one of the most common genetic causes of mental retardation in girls. __MECP2__ point mutations in exons 2–4 account for about 80% of classic Rett cases and for a lower percentage of variant patients. We investigated the gen

MeCP2: Making sense of missense in Rett
MeCP2: Making sense of missense in Rett syndrome
✍ Banerjee, Abhishek; Romero-Lorenzo, Esmeralda; Sur, Mriganka πŸ“‚ Article πŸ“… 2013 πŸ› Nature Publishing Group 🌐 English βš– 417 KB