Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21
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J. Gilbert | M. Pericak-Vance | J. Vance | J. Stajich | C. Hulette | M. Hamida | J. E. Stenger | F. Hentati | J. Rochelle | K. B. Othmane | S. Dew-Knight | R. Baxter | S. Bel | J. Gilbert | K. Othmane
[1] I. Marín,et al. The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease , 2002, Nature Genetics.
[2] M. Hamida,et al. Linkage of a new locus for autosomal recessive axonal form of Charcot–Marie–Tooth disease to chromosome 8q21.3 , 2001, Neuromuscular Disorders.
[3] J. Vance. The many faces of Charcot-Marie-Tooth disease. , 2000, Archives of neurology.
[4] M. Pericak-Vance,et al. Fine localization of the CMT4A locus using a PAC contig and haplotype analysis , 1998, Neurogenetics.
[5] C. van Broeckhoven,et al. Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease , 2006 .
[6] M. Pericak-Vance,et al. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. , 1993, Human molecular genetics.
[7] M. Colombo,et al. Isolation and mapping to 17p12-13 of the human homologous of the murine growth arrest specific Gas-3 gene. , 1992, Human molecular genetics.
[8] P. Dyck,et al. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations. , 1968, Archives of neurology.
[9] P. Dyck,et al. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. , 1968, Archives of neurology.