The many faces of Charcot-Marie-Tooth disease

[11] HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED - A HALF CENTURY FOLLOW-UP [J]. NEUROLOGY, 1987, 37 (09) : 1460 - 1465

[12] Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15 [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 161 (01) : 23 - 28

[13] X-linked dominant Charcot-Marie-Tooth disease:: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln) [J]. ACTA NEUROPATHOLOGICA, 1998, 95 (05) : 443 - 449

[14] SENDEREK J, 1999, EUR CHARC MAR TOOTH

[15] Distal hereditary motor neuropathy type II (distal HMN II): Mapping of a locus to chromosome 12q24 [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (07) : 1065 - 1069

[16] VANCE JM, 1997, AM AC NEUR M APR 17

[17] Charcot-Marie-Tooth disease: an intermediate form [J]. NEUROMUSCULAR DISORDERS, 1998, 8 (06) : 392 - 393

[11] HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED - A HALF CENTURY FOLLOW-UP [J]. NEUROLOGY, 1987, 37 (09) : 1460 - 1465

[12] Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15 [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 161 (01) : 23 - 28

[13] X-linked dominant Charcot-Marie-Tooth disease:: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln) [J]. ACTA NEUROPATHOLOGICA, 1998, 95 (05) : 443 - 449

[14] SENDEREK J, 1999, EUR CHARC MAR TOOTH

[15] Distal hereditary motor neuropathy type II (distal HMN II): Mapping of a locus to chromosome 12q24 [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (07) : 1065 - 1069

[16] VANCE JM, 1997, AM AC NEUR M APR 17

[17] Charcot-Marie-Tooth disease: an intermediate form [J]. NEUROMUSCULAR DISORDERS, 1998, 8 (06) : 392 - 393