A mutation associated with CMT2A neuropathy causes defects in Fzo1 GTP hydrolysis, ubiquitylation, and protein turnover. (Q27939124)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A mutation associated with CMT2A neuropathy causes defects in Fzo1 GTP hydrolysis, ubiquitylation, and protein turnover. |
scientific article |
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A mutation associated with CMT2A neuropathy causes defects in Fzo1 GTP hydrolysis, ubiquitylation, and protein turnover (English)
Elizabeth A Amiott
Allan M Weissman
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