DIAGNOSTIC-CRITERIA FOR AUTOSOMAL-DOMINANT HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-IA

[1] CHANCE PF, 1990, AM J HUM GENET, V47, P915

[2] CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION [J]. HUMAN GENETICS, 1991, 88 (01) : 1 - 12

[3] PERIPHERAL MYELIN PROTEIN-22 GENE MAPS IN THE DUPLICATION IN CHROMOSOME-17P11.2 ASSOCIATED WITH CHARCOT-MARIE-TOOTH-1A [J]. NATURE GENETICS, 1992, 1 (03) : 176 - 179

[4] THE GENE FOR THE PERIPHERAL MYELIN PROTEIN-PMP-22 IS A CANDIDATE FOR CHARCOT-MARIE-TOOTH DISEASE TYPE-1A [J]. NATURE GENETICS, 1992, 1 (03) : 159 - 165

[5] Raeymaekers P, 1991, Neuromuscul Disord, V1, P93, DOI 10.1016/0960-8966(91)90055-W

[6] A LEUCINE-TO-PROLINE MUTATION IN THE PUTATIVE 1ST TRANSMEMBRANE DOMAIN OF THE 22-KDA PERIPHERAL MYELIN PROTEIN IN THE TREMBLER-J MOUSE [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) : 4382 - 4386

[7] TREMBLER MOUSE CARRIES A POINT MUTATION IN A MYELIN GENE [J]. NATURE, 1992, 356 (6366) : 241 - 244

[8] THE PERIPHERAL MYELIN PROTEIN GENE PMP-22 IS CONTAINED WITHIN THE CHARCOT-MARIE-TOOTH DISEASE TYPE-1A DUPLICATION [J]. NATURE GENETICS, 1992, 1 (03) : 171 - 175

[9] THE PERIPHERAL MYELIN GENE PMP-22/GAS-3 IS DUPLICATED IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1A [J]. NATURE GENETICS, 1992, 1 (03) : 166 - 170

[10] LINKAGE OF CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-1A TO CHROMOSOME-17 [J]. EXPERIMENTAL NEUROLOGY, 1989, 104 (02) : 186 - 189

[1] CHANCE PF, 1990, AM J HUM GENET, V47, P915

[2] CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION [J]. HUMAN GENETICS, 1991, 88 (01) : 1 - 12

[3] PERIPHERAL MYELIN PROTEIN-22 GENE MAPS IN THE DUPLICATION IN CHROMOSOME-17P11.2 ASSOCIATED WITH CHARCOT-MARIE-TOOTH-1A [J]. NATURE GENETICS, 1992, 1 (03) : 176 - 179

[4] THE GENE FOR THE PERIPHERAL MYELIN PROTEIN-PMP-22 IS A CANDIDATE FOR CHARCOT-MARIE-TOOTH DISEASE TYPE-1A [J]. NATURE GENETICS, 1992, 1 (03) : 159 - 165

[5] Raeymaekers P, 1991, Neuromuscul Disord, V1, P93, DOI 10.1016/0960-8966(91)90055-W

[6] A LEUCINE-TO-PROLINE MUTATION IN THE PUTATIVE 1ST TRANSMEMBRANE DOMAIN OF THE 22-KDA PERIPHERAL MYELIN PROTEIN IN THE TREMBLER-J MOUSE [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) : 4382 - 4386

[7] TREMBLER MOUSE CARRIES A POINT MUTATION IN A MYELIN GENE [J]. NATURE, 1992, 356 (6366) : 241 - 244

[8] THE PERIPHERAL MYELIN PROTEIN GENE PMP-22 IS CONTAINED WITHIN THE CHARCOT-MARIE-TOOTH DISEASE TYPE-1A DUPLICATION [J]. NATURE GENETICS, 1992, 1 (03) : 171 - 175

[9] THE PERIPHERAL MYELIN GENE PMP-22/GAS-3 IS DUPLICATED IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1A [J]. NATURE GENETICS, 1992, 1 (03) : 166 - 170

[10] LINKAGE OF CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-1A TO CHROMOSOME-17 [J]. EXPERIMENTAL NEUROLOGY, 1989, 104 (02) : 186 - 189