Tuschl et al., 2016 - Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia. Nature communications   7:11601 Full text @ Nat. Commun.
4 Genes / Markers
Marker Type Symbol Name
Gene slc11a2 solute carrier family 11 member 2
Gene slc39a14 solute carrier family 39 member 14
Gene slc39a8 solute carrier family 39 member 8
Gene tfr1a transferrin receptor 1a
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.