The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype (Q48267649)
scientific article published in February 1999
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Current Data About The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype
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(P1476) "The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype" (language: en)
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Timmerman V
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Ceuterick C
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Nelis E
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De Vriendt E
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Löfgren A
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Vercruyssen A
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Verellen C
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Van Maldergem L
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Martin JJ
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other details
description scientific article published in February 1999

External Links
(P356) 10.1093/BRAIN/122.2.281
(P698) 10071056
(P5875) 237807974