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J Neurol. 2015 Dec;262(12):2776-9. doi: 10.1007/s00415-015-7955-5. Epub 2015 Nov 3.

Mitochondrial DNA mutation 14487T>C manifesting as Leber's hereditary optic neuropathy.

Author information

1
Department of Neuropediatrics and Muscle Disorders, University Center for Pediatrics Freiburg, Mathildenstr. 1, 79106, Freiburg, Germany. matthias.eckenweiler@uniklinik-freiburg.de.
2
Friedrich-Baur-Institut an der Neurologischen Klinik, Klinikum der Universität München, Munich, Germany. claudia.catarino@med.uni-muenchen.de.
3
Friedrich-Baur-Institut an der Neurologischen Klinik, Klinikum der Universität München, Munich, Germany. constanze.gallenmueller@gmx.net.
4
Friedrich-Baur-Institut an der Neurologischen Klinik, Klinikum der Universität München, Munich, Germany. tklopsto@med.lmu.de.
5
Eye Center at the Medical Center, University of Freiburg, Freiburg, Germany. wolf.lagreze@uniklinik-freiburg.de.
6
Department of Neuropediatrics and Muscle Disorders, University Center for Pediatrics Freiburg, Mathildenstr. 1, 79106, Freiburg, Germany. rudolf.korinthenberg@uniklinik-freiburg.de.
7
Department of Neuropediatrics and Muscle Disorders, University Center for Pediatrics Freiburg, Mathildenstr. 1, 79106, Freiburg, Germany. janbernd.kirschner@uniklinik-freiburg.de.
PMID:
26530508
DOI:
10.1007/s00415-015-7955-5
[Indexed for MEDLINE]

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