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About this Biochemistry, Genetics and Molecular Biology article
A novel deletion–insertion mutation identified in exon 3 of FXN in two siblings with a severe Friedreich ataxia phenotype by Marguerite V. Evans-Galea; Louise A. Corben; Justin Hasell; Charles A. Galea; Michael C. Fahey; Desirée du Sart; Martin B. Delatycki 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
- Marguerite V. Evans-Galea; Louise A. Corben; Justin Hasell; Charles A. Galea; Michael C. Fahey; Desirée du Sart; Martin B. Delatycki
- Publisher
- Springer; Springer-Verlag; Springer Verlag; Springer Science and Business Media LLC; Springer Nature (ISSN 1364-6745)
- Published
- 2011
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)