Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity
Heussinger, Nicole, Saake, Marc, Mennecke, Angelika, Dörr, Helmuth-Günther, Trollmann, ReginaVolume:
67
Language:
english
Journal:
Pediatric Neurology
DOI:
10.1016/j.pediatrneurol.2016.10.007
Date:
February, 2017
File:
PDF, 1.73 MB
english, 2017