Editorial: Neuronopathic lysosomal storage diseases - specific neuronal characteristics and therapeutic approaches

Front Mol Neurosci. 2022 Nov 8:15:1078804. doi: 10.3389/fnmol.2022.1078804. eCollection 2022.

Authors

Stefanie Flunkert^{1

2}, Birgit Hutter-Paier¹, Ying Sun^{3

4}, Jan Kehr^{5

6}

Affiliations

¹ QPS Austria, Grambach, Austria.
² BioDoks e.U., St. Georgen an der Stiefing, Austria.
³ Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
⁴ Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
⁵ Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
⁶ Pronexus Analytical SA, Bromma, Sweden.

No abstract available

Keywords: Krabbe disease; TFEB; animal models; mTORC1; neuronopathic Gaucher disease; umbilical cord blood transplantation (UCBT).

Publication types

Editorial