𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutational screening ofARXgene in Brazilian males with mental retardation of unknown etiology

✍ Scribed by Raquel de Souza Gestinari-Duarte; Cíntia Barros Santos-Rebouças; Márcia Mattos Gonçalves Pimentel


Publisher
Nature Publishing Group
Year
2006
Tongue
English
Weight
150 KB
Volume
51
Category
Article
ISSN
1435-232X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Identification of a family with nonspeci
✍ Birgitta Winnepenninckx; Vanessa Errijgers; France Hayez-Delatte; Edwin Reyniers 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 126 KB

Mutations in the methyl-CpG-binding protein 2 (MECP2) cause Rett syndrome, a severe neurodevelopmental disorder occurring predominantly in females. Male patients with Rett syndrome are extremely rare, as the Rett-causing mutations in the MECP2 gene are usually lethal in hemizygous males. However, di