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About this Biochemistry, Genetics and Molecular Biology article
SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype by Bugiardini, E.; Rivolta, I.; Binda, A.; Soriano Caminero, A.; Cirillo, F.; Cinti, A.; Giovannoni, R.; Botta, A.; Cardani, R.; Wicklund, M.P.; Meola, G. is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Bugiardini, E.; Rivolta, I.; Binda, A.; Soriano Caminero, A.; Cirillo, F.; Cinti, A.; Giovannoni, R.; Botta, A.; Cardani, R.; Wicklund, M.P.; Meola, G.
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 0960-8966)
- Published
- 2015
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)