Mutation Analysis Provides Additional Proof That Mottled is the Mouse Homologue of Menkes' Disease

By Reed Vivienne   Boyd Yvonne  

Human Molecular Genetics, Vol. 6, Iss. 3, 1997-01 ,pp. : 417-423

Oxford University Press

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Molecular Basis of the Brindled Mouse Mutant ( Mobr ): A Murine Model of Menkes Disease

By Grimes Andrew   Hearn Catherine J.   Lockhart Paul   Newgreen Don F.   Mercer Julian F. B.  

Human Molecular Genetics, Vol. 6, Iss. 7, 1997-01 ,pp. : 1037-1042

Oxford University Press

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Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing

By Ferenci Peter  

Human Genetics, Vol. 120, Iss. 2, 2006-09 ,pp. : 151-159

Springer Publishing Company

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The Menkes disease ATPase (ATP7A) is internalized via a Rac1-regulated, clathrin- and caveolae-independent pathway

By Cobbold C.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1523-1533

Oxford University Press

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Constitutive skipping of alternatively spliced exon 10 in the ATP7A gene abolishes Golgi localization of the Menkes protein and produces the occipital horn syndrome

By Qi M.   Byers P.H.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 465-469

Oxford University Press

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