Cite
HARVARD Citation
Verrigni, D. et al. (2019). Clinical‐genetic features and peculiar muscle histopathology in infantile DNM1L‐related mitochondrial epileptic encephalopathy. Human mutation. 40 (5), pp. 601-618. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Verrigni, D. et al. (2019). Clinical‐genetic features and peculiar muscle histopathology in infantile DNM1L‐related mitochondrial epileptic encephalopathy. Human mutation. 40 (5), pp. 601-618. [Online].