(Q48408036)
Statements
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Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation. (English)
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Gabreëls FJ
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Lenssen PP
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Gabreëls-Festen AA
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Valentijn LJ
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Jongen PJ
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van Beersum SE
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van Engelen BG
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van Wensen PJ
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Bolhuis PA
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Mariman EC
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1 August 1998
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121 ( Pt 8)
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1451-1458
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Identifiers
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