Article
Loss of <i>slc39a14</i> causes simultaneous manganese deficiency and hypersensitivity in zebrafish
2020-01-31
Abstract excerpt
Mutations in SLC39A14, a manganese uptake transporter, lead to a neurodegenerative disorder characterised by accumulation of manganese in the brain and rapidly progressive dystonia-parkinsonism (Hypermanganesemia with Dystonia 2, HMNDYT2). Similar to the human phenotype, zebrafish slc39a14 U801-/- mutants show prominent brain manganese accumulation and abnormal locomotor behaviour. In order to identify novel pot...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 7891ec58-9f50-5fac-9c68-ee267699bed6
- DOI
- 10.1101/2020.01.31.921130
