(Q46193499)
Statements
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A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease (English)
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Kessali M
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Zemmouri R
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Guilbot A
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Maisonobe T
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Brice A
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LeGuern E
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Grid D
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1 April 1997
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48
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4
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867-873
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Identifiers
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