About this Biochemistry, Genetics and Molecular Biology article
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leight syndrome (MILS) associated with the mtDNA T8993G point mutation by F. Degoul; M. Diry; D. Rodriguez; O. Robain; D. François; G. Ponsot; C. Marsac; I. Desguerre 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
- F. Degoul; M. Diry; D. Rodriguez; O. Robain; D. François; G. Ponsot; C. Marsac; I. Desguerre
- Publisher
- Springer; Wiley (John Wiley & Sons); Kluwer Academic Publishers; Wiley; Springer Science and Business Media LLC (ISSN 0141-8955)
- Published
- 1995
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)