Back to search

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
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Loss of <i>slc39a14</i> causes simultaneous manganese deficiency and hypersensitivity in zebrafishDOI 10.1101/2020.01.31.921130
Select a neighboring publication to make it the new centre.