%0 Journal Article
%T PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristics
%J -
%D 2019
%R https://doi.org/10.1038/s41436-019-0512-3
%X To provide a detailed electroclinical description and expand the phenotype of PIGT-CDG, to perform genotype¨Cphenotype correlation, and to investigate the onset and severity of the epilepsy associated with the different genetic subtypes of this rare disorder. Furthermore, to use computer-assisted facial gestalt analysis in PIGT-CDG and to the compare findings with other glycosylphosphatidylinositol (GPI) anchor deficiencies
%U https://www.nature.com/articles/s41436-019-0512-3