TY  - GEN
AU  - Sell,Katharina
AU  - Storch,Katja
AU  - Hahn,Gabriele
AU  - Lee-Kirsch,Min Ae
AU  - Ramantani,Georgia
AU  - Jackson,Sandra
AU  - Neilson,Derek
AU  - von der Hagen,Maja
AU  - Hehr,Ute
AU  - Smitka,Martin
TI  - Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation
SN  - 1872-7131
PY  - 2017///0117
KW  - Brain
KW  - diagnostic imaging
KW  - Diagnosis, Differential
KW  - Humans
KW  - Infant
KW  - Leukoencephalitis, Acute Hemorrhagic
KW  - diagnosis
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Molecular Chaperones
KW  - genetics
KW  - Mutation, Missense
KW  - Nuclear Pore Complex Proteins
KW  - Phenotype
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.braindev.2016.02.007
ER  -