SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency. (Q47851457)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency. |
scientific article |
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SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency. (English)
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Stephan Zuchner
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Adriana P Rebelo
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Dimah Saade
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Amjad Farooq
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Tyler C Huff
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Lisa Abreu
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Carlos T Moraes
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Diana Mnatsakanova
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Kathy Mathews
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Hua Yang
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Eric A Schon
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16 January 2018
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