| Literature DB >> 7566463 |
Abstract
Rett syndrome is a progressive neurological development syndrome. Evidences for a genetic transmission, but no conclusive data which entirely support the X chromosome involvement, exist. The chromosomal region 11p14-pte has been investigated with polymorphic markers and genes in the region have been sequenced. No sequence divergencies were detected.Entities:
Mesh：
Year: 1995 PMID： 7566463 DOI： 10.1055/s-2007-979733
Source DB: PubMed Journal: Neuropediatrics ISSN： 0174-304X Impact factor: 1.947