A Novel Frameshift Mutation in Exon 23 of ATP7A (MNK) Results in Occipital Horn Syndrome and Not in Menkes Disease

por Dagenais, Susan L., Adam, Ayla N., Innis, Jeffrey W., Glover, Thomas W.
Publicado 2001

Immunocytochemical Localization of the Menkes Copper Transport Protein (ATP7A) to the Trans-Golgi Network

por Dierick, Herman A., Adam, Ayla N., Escara-Wilke, June F., Glover, Thomas W.
Publicado en Hum Mol Genet (1997)