Cite
HARVARD Citation
Liu, Z. et al. (2022). Whole genome and exome sequencing identify NDUFV2 mutations as a new cause of progressive cavitating leukoencephalopathy. Journal of medical genetics. 59 (4), pp. 351-357. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Liu, Z. et al. (2022). Whole genome and exome sequencing identify NDUFV2 mutations as a new cause of progressive cavitating leukoencephalopathy. Journal of medical genetics. 59 (4), pp. 351-357. [Online].