Behr syndrome with homozygous C19ORF12 mutation.
Kleffner I, Wessling C, Gess B, Korsukewitz C, Allkemper T, Schirmacher A, Young P, Senderek J, Husstedt IW.
Kleffner I, et al. Among authors: gess b.
J Neurol Sci. 2015 Oct 15;357(1-2):115-8. doi: 10.1016/j.jns.2015.07.009. Epub 2015 Jul 9.
J Neurol Sci. 2015.
PMID: 26187298