| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8276445 | Journal of the Neurological Sciences | 2015 | 5 Pages |
Abstract
C19orf12 mutations were confirmed in our heterogeneous NBIA cohort, while WDR45 mutations appear to be restricted to the subtype showing encephalopathy in childhood with neurodegeneration in adulthood.
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Ageing
Authors
Anne Tschentscher, Gabriele Dekomien, Sophia Ross, Kirsten Cremer, Guido M. Kukuk, Jörg T. Epplen, Sabine Hoffjan,