UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis. [electronic resource]
Producer: 20121129Description: 2230.e1-2230.e5 p. digitalISSN:- 1558-1497
- Adaptor Proteins, Signal Transducing
- Amyotrophic Lateral Sclerosis -- genetics
- Animals
- Autophagy-Related Proteins
- Canada
- Cell Cycle Proteins -- genetics
- Computational Biology
- DNA Mutational Analysis
- Female
- Genetic Predisposition to Disease -- genetics
- Humans
- Male
- Mutation, Missense -- genetics
- Ubiquitins -- genetics
- White People -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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