CLONING THE WILSON DISEASE GENE

[1] THE WILSON DISEASE GENE IS A PUTATIVE COPPER TRANSPORTING P-TYPE ATPASE SIMILAR TO THE MENKES GENE [J]. NATURE GENETICS, 1993, 5 (04) : 327 - 337

[2] Bush A. J., 1993, Society for Neuroscience Abstracts, V19, P19

[3] ISOLATION OF A CANDIDATE GENE FOR MENKES DISEASE THAT ENCODES A POTENTIAL HEAVY-METAL BINDING-PROTEIN [J]. NATURE GENETICS, 1993, 3 (01) : 14 - 19

[4] Danks DM, 1989, METABOLIC BASIS INHE, P1411

[5] ASSIGNMENT OF THE GENE FOR WILSON DISEASE TO CHROMOSOME-13 - LINKAGE TO THE ESTERASE-D LOCUS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (06) : 1819 - 1821

[6] ISOLATION OF A PARTIAL CANDIDATE GENE FOR MENKES DISEASE BY POSITIONAL CLONING [J]. NATURE GENETICS, 1993, 3 (01) : 20 - 25

[7] MAPPING, CLONING AND GENETIC-CHARACTERIZATION OF THE REGION CONTAINING THE WILSON DISEASE GENE [J]. NATURE GENETICS, 1993, 5 (04) : 338 - 343

[8] DEFICIENCY OF CERULOPLASMIN IN PATIENTS WITH HEPATOLENTICULAR DEGENERATION (WILSONS DISEASE) [J]. SCIENCE, 1952, 116 (3018) : 484 - 485

[9] HUMAN MENKES X-CHROMOSOME DISEASE AND THE STAPHYLOCOCCAL CADMIUM-RESISTANCE ATPASE - A REMARKABLE SIMILARITY IN PROTEIN SEQUENCES [J]. MOLECULAR MICROBIOLOGY, 1993, 10 (01) : 7 - 12

[10] THE WILSON DISEASE GENE IS A COPPER TRANSPORTING ATPASE WITH HOMOLOGY TO THE MENKES DISEASE GENE [J]. NATURE GENETICS, 1993, 5 (04) : 344 - 350

[1] THE WILSON DISEASE GENE IS A PUTATIVE COPPER TRANSPORTING P-TYPE ATPASE SIMILAR TO THE MENKES GENE [J]. NATURE GENETICS, 1993, 5 (04) : 327 - 337

[2] Bush A. J., 1993, Society for Neuroscience Abstracts, V19, P19

[3] ISOLATION OF A CANDIDATE GENE FOR MENKES DISEASE THAT ENCODES A POTENTIAL HEAVY-METAL BINDING-PROTEIN [J]. NATURE GENETICS, 1993, 3 (01) : 14 - 19

[4] Danks DM, 1989, METABOLIC BASIS INHE, P1411

[5] ASSIGNMENT OF THE GENE FOR WILSON DISEASE TO CHROMOSOME-13 - LINKAGE TO THE ESTERASE-D LOCUS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (06) : 1819 - 1821

[6] ISOLATION OF A PARTIAL CANDIDATE GENE FOR MENKES DISEASE BY POSITIONAL CLONING [J]. NATURE GENETICS, 1993, 3 (01) : 20 - 25

[7] MAPPING, CLONING AND GENETIC-CHARACTERIZATION OF THE REGION CONTAINING THE WILSON DISEASE GENE [J]. NATURE GENETICS, 1993, 5 (04) : 338 - 343

[8] DEFICIENCY OF CERULOPLASMIN IN PATIENTS WITH HEPATOLENTICULAR DEGENERATION (WILSONS DISEASE) [J]. SCIENCE, 1952, 116 (3018) : 484 - 485

[9] HUMAN MENKES X-CHROMOSOME DISEASE AND THE STAPHYLOCOCCAL CADMIUM-RESISTANCE ATPASE - A REMARKABLE SIMILARITY IN PROTEIN SEQUENCES [J]. MOLECULAR MICROBIOLOGY, 1993, 10 (01) : 7 - 12

[10] THE WILSON DISEASE GENE IS A COPPER TRANSPORTING ATPASE WITH HOMOLOGY TO THE MENKES DISEASE GENE [J]. NATURE GENETICS, 1993, 5 (04) : 344 - 350