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Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity
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1993
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BiologyMendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyChromosome 1PPathologyMolecular GeneticsGenetic VariationGenetic HeterogeneityDisease Gene IdentificationPublic HealthMedicineMonogenic Disorders
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