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Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
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The Roussy-Levy Family:From the Original Description to the Gene
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
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