Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
Mencarelli MA; Spanhol-Rosseto A; Artuso R; Rondinella D; De Filippis R; Bahi-Buisson N; Nectoux J; Rubinsztajn R; Bienvenu T; Moncla A; Chabrol B; Villard L; Krumina Z; Armstrong J; Roche A; Pineda M; Gak E; Mari F; Ariani F; Renieri A; Journal Of Medical Genetics, 2010, vol. 47, issue 1, p 49, ISSN 14686244. ISBN 14686244.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef