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About this Biochemistry, Genetics and Molecular Biology article
The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrence by Vilma-Lotta Lehtokari; Rebecca S. Greenleaf; Elizabeth T. DeChene; Mutsumi Kellinsalmi; Katarina Pelin; Nigel G. Laing; Alan H. Beggs; Carina Wallgren-Pettersson 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
- Vilma-Lotta Lehtokari; Rebecca S. Greenleaf; Elizabeth T. DeChene; Mutsumi Kellinsalmi; Katarina Pelin; Nigel G. Laing; Alan H. Beggs; Carina Wallgren-Pettersson
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 0960-8966)
- Published
- 2009
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)