Overlap Phenotype between CMT1A and Hereditary Neuropathy with Liability to Pressure Palsies Caused by the Novel Small In-frame Deletion c.407_418del12 in PMP22 Gene
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1997 ◽
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pp. 274-286
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2015 ◽
Vol 42
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pp. S15-S15
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2005 ◽
Vol 15
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pp. 493-497
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Vol 12
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pp. 651-655
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pp. 348-354
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Vol 263
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pp. 194-197
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