Cite
HARVARD Citation
Debray, F. et al. (2011). LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency. Journal of medical genetics. 48 (3), pp. 183-189. [Online].
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Debray, F. et al. (2011). LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency. Journal of medical genetics. 48 (3), pp. 183-189. [Online].