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About this Biochemistry, Genetics and Molecular Biology article
A third case of congenital myasthenic syndrome caused by mutations in SCN4A by Witting, N.; Werlauff, U.; Ballegaard, M.; Vissing, J. 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
- Witting, N.; Werlauff, U.; Ballegaard, M.; Vissing, J.
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 0960-8966)
- Published
- 2015
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)
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