(Q46786595)
Statements
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Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C. (English)
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Tazir M
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Azzedine H
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Assami S
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Sindou P
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Nouioua S
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Zemmouri R
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Hamadouche T
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Chaouch M
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Feingold J
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Vallat JM
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Leguern E
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Grid D
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7 November 2003
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127
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Pt 1
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154-163
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Identifiers
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