Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings

R. J. Oostra, C. van den Bogert, L. G. Nijtmans, M. J. van Galen, R. Zwart, P. A. Bolhuis, E. M. Bleeker-Wagemakers

Research output: Contribution to journalComment/Letter to the editorAcademic

12 Citations (Scopus)
Original languageEnglish
Pages (from-to)954-957
JournalAmerican journal of human genetics
Volume57
Issue number4
Publication statusPublished - 1995

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