Knockin mouse model of the human CFL2 p.A35T mutation results in a unique splicing defect and severe myopathy phenotype. [electronic resource]
Producer: 20210823Description: 1996-2003 p. digitalISSN:- 1460-2083
- Actins -- metabolism
- Animals
- Cofilin 2 -- genetics
- Disease Models, Animal
- Gene Knock-In Techniques
- Genetic Predisposition to Disease
- Humans
- Mice
- Mice, Knockout
- Microfilament Proteins -- genetics
- Muscle, Skeletal -- metabolism
- Muscular Diseases -- genetics
- Mutation -- genetics
- Phenotype
- RNA, Messenger -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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