A mutation associated with CMT2A neuropathy causes defects in Fzo1 GTP hydrolysis, ubiquitylation, and protein turnover. (Q27939124)
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scientific article
| 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 |
Statements
A mutation associated with CMT2A neuropathy causes defects in Fzo1 GTP hydrolysis, ubiquitylation, and protein turnover (English)
Elizabeth A Amiott
Allan M Weissman
Janet M Shaw
7 October 2009
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