| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8275385 | Journal of the Neurological Sciences | 2015 | 4 Pages |
Abstract
We expand the spectrum of genetic causes of Behr syndrome. Genetic testing of patients presenting with Behr syndrome should include C19ORF12 mutation screening.
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Authors
Ilka Kleffner, Caroline Wessling, Burkhard Gess, Catharina Korsukewitz, Thomas Allkemper, Anja Schirmacher, Peter Young, Jan Senderek, Ingo W. Husstedt,