A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype
Romaniello, Romina, Saettini, Francesco, Panzeri, Elena, Arrigoni, Filippo, Bassi, Maria T., Borgatti, RenatoVolume:
26
Language:
english
Journal:
NeuroReport
DOI:
10.1097/WNR.0000000000000337
Date:
March, 2015
File:
PDF, 152 KB
english, 2015