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Loss of slc39a14 causes simultaneous manganese deficiency and hypersensitivity in zebrafish (2020)

First Author: Tuschl K

Attributed to: Resolving the basis of phenotypically variable hereditary abnormalities of eye formation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/2020.01.31.921130

Publication URI: http://dx.doi.org/10.1101/2020.01.31.921130

Type: Preprint