The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype (Q48267649)
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scientific article published in February 1999
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype |
scientific article published in February 1999 |
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The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype (English)
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Van Broeckhoven C
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De Jonghe P
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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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1 February 1999
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122 ( Pt 2)
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281-290
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