A Golgi localization signal identified in the Menkes recombinant protein.
Menkes disease arises from a genetic impairment in copper transport. The gene responsible for the phenotype has been identified as a copper transporting ATPase ( ATP7A ). Recently, the protein encoded by the ATP7A gene has been localized to the Golgi complex. In order to investigate the role of the...
Main Authors: | Francis, M, Jones, E, Levy, E, Ponnambalam, S, Chelly, J, Monaco, A |
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Format: | Journal article |
Language: | English |
Published: |
1998
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