(Q44852766)
Statements
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A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness (English)
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In Soo Joo
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Sung Yeol Joo
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Kyoon Huh
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Jong-Won Kim
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1 May 2004
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14
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5
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325-328
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Identifiers
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