NTNG1 mutations are a rare cause of Rett syndrome

A translocation that disrupted the netrin G1 gene (NTNG1) was recently reported in a patient with the early seizure variant of Rett syndrome (RTT).

Authors:
Archer HL, Evans JC, Millar DS, Thompson PW, Kerr AM, Leonard H, Christodoulou J, Ravine D, Lazarou L, Grove L, Verity C, Whatley SD, Pitz DT, Sampson JR, Clarke AJ

Authors notes:
American Journal of Medical Genetics Part A. 2006; 140A(7):691-694

Keywords:
NTNG1 mutations, rare, Rett syndrome

Abstract:
A translocation that disrupted the netrin G1 gene (NTNG1) was recently reported in a patient with the early seizure variant of Rett syndrome (RTT).