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Updated: Apr 20, 2026

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
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Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease
Tsz Hang Wong1, Annemieke J M H Verkerk2, Annemieke J Rozemuller3
11 Department of Neurology, Erasmus Medical Centre, 3015 CE Rotterdam, The Netherlands.
Brain : a Journal of Neurology
|November 22, 2014
Abstract
No abstract available in PubMed .
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