Cite
HARVARD Citation
Lou, X. et al. (2018). A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome. Journal of human genetics. 63 (12), pp. 1269-1272. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Lou, X. et al. (2018). A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome. Journal of human genetics. 63 (12), pp. 1269-1272. [Online].