Clinical, biochemical, and molecular analysis of a...

Journal of Inherited Metabolic Disease 1995 Vol. 18; Iss. 6

Clinical, biochemical, and molecular analysis of a maternally inherited case of Leight syndrome (MILS) associated with the mtDNA T8993G point mutation

F. Degoul, M. Diry, D. Rodriguez, O. Robain, D. François, G. Ponsot, C. Marsac, I. Desguerre
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Volume:
18
Year:
1995
Language:
english
Pages:
7
DOI:
10.1007/bf02436757
File:
PDF, 629 KB
english, 1995
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