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Characterization of the exon structure of the Menkes disease gene using vectorette PCR

Archive ouverte | Tümer, Zeynep | CCSD

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A Golgi localization signal identified in the Menkes recombinant protein

Archive ouverte | Francis, Michael J. | CCSD

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 lo...

DXS106 and DXS559 Flank the X-Linked Dystonia-Parkinsonism Syndrome Locus (DYT3)

Archive ouverte | Müller, Ulrich | CCSD

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