Abstract
We describe sequence analysis of the mitochondrial DNA of five Hungarian patients diagnosed with probable LHON, who do not carry any of the three primary point mutations. We report three novel mutations, one of which might have a pathogenic role.
Cite
CITATION STYLE
APA
Horvath, J., Horvath, R., Karcagi, V., Komoly, S., & Johns, D. R. (2002). Sequence analysis of Hungarian LHON patients not carrying the common primary mutations. Journal of Inherited Metabolic Disease, 25(4), 323–324. https://doi.org/10.1023/A:1016518811940
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